KONICAMINOLTA DI-X1
Summary
Konica Minolta, Inc. received 510(k) clearance for KONICAMINOLTA DI-X1, a LLZ device. Cleared on 2021-09-13.
Details
Source
510(k) Clearance
External ID
K212685
Action Date
2021-09-13
Status
Special
Category
device
Product Code
LLZ
Product Description
KONICAMINOLTA DI-X1. Product code: LLZ.
Company
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. Konica Minolta, Inc. has received 9 total clearances in our database.
Konica Minolta, Inc. has 9 FDA actions in our database, including 9 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 Konica Minolta, Inc. have FDA actions?
Konica Minolta, Inc. has 9 FDA actions in our database, including 0 recalls and 9 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K212685" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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