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FDA 510(k)

DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH

K-Number: K881332 · 1988-04-27

ApplicantBaxter Healthcare Corp
Decision Date1988-04-27
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1988-04-27 under 510(k) number K881332. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH?

DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH is a medical device that received FDA 510(k) clearance on 1988-04-27. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K881332.

When did DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH receive FDA 510(k) clearance?

DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH received FDA 510(k) clearance on 1988-04-27, under 510(k) number K881332.

Who is the listed applicant for DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH?

The FDA product code for DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH is OCZ.

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Related Devices (Code: OCZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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