RecallHawk

NOVEOS Specific IgE (sIgE); Capture Reagent F024, Shrimp (Shrimp spp.); Capture Reagent F207, Clam (Mercenaria mercenari

Hycor Biomedical

Summary

Hycor Biomedical received 510(k) clearance for NOVEOS Specific IgE (sIgE); Capture Reagent F024, Shrimp (Shrimp spp.); Capture Reagent F207, Clam (Mercenaria mercenaria); Capture Reagent F256, Walnut (Juglans spp.) ; Capture Reagent I006, German Cockroach (Blatella germanica), a DHB device. Cleared on 2025-12-23.

Details

Source

510(k) Clearance

External ID

K252493

Action Date

2025-12-23

Status

Traditional

Category

device

Product Code

DHB

Product Description

NOVEOS Specific IgE (sIgE); Capture Reagent F024, Shrimp (Shrimp spp.); Capture Reagent F207, Clam (Mercenaria mercenaria); Capture Reagent F256, Walnut (Juglans spp.) ; Capture Reagent I006, German Cockroach (Blatella germanica). Product code: DHB.

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. Hycor Biomedical has received 6 total clearances in our database.

Hycor Biomedical has 6 FDA actions in our database, including 6 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 Hycor Biomedical have FDA actions?

Hycor Biomedical has 6 FDA actions in our database, including 0 recalls and 6 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K252493" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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