Single Use Hand Switch Monopolar Forceps with Smoke Evacuation, Single Use Hand Switch Bipolar Forceps with Smoke Evacua
Summary
Modern Medical Equipment Manufacturing, Ltd. received 510(k) clearance for Single Use Hand Switch Monopolar Forceps with Smoke Evacuation, Single Use Hand Switch Bipolar Forceps with Smoke Evacuation, Single Use Hand Switch Monopolar Forceps, Single Use Hand Switch Bipolar Forceps, a GEI device. Cleared on 2022-03-17.
Details
Source
510(k) Clearance
External ID
K210315
Action Date
2022-03-17
Status
Traditional
Category
device
Product Code
GEI
Product Description
Single Use Hand Switch Monopolar Forceps with Smoke Evacuation, Single Use Hand Switch Bipolar Forceps with Smoke Evacuation, Single Use Hand Switch Monopolar Forceps, Single Use Hand Switch Bipolar Forceps. Product code: GEI.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Modern Medical Equipment Manufacturing, Ltd. has received 2 total clearances in our database.
Modern Medical Equipment Manufacturing, Ltd. has 2 FDA actions in our database, including 2 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Modern Medical Equipment Manufacturing, Ltd. have FDA actions?
Modern Medical Equipment Manufacturing, Ltd. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K210315" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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