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FDA 510(k)

FLEXIBLE BIOPSY FORCEP

K-Number: K871809 · 1987-06-18

Decision Date1987-06-18
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE BIOPSY FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is Surgi-Aid Endoscopics, Inc.. It received FDA 510(k) clearance on 1987-06-18 under 510(k) number K871809. 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 FLEXIBLE BIOPSY FORCEP?

FLEXIBLE BIOPSY FORCEP is a medical device that received FDA 510(k) clearance on 1987-06-18. The listed applicant is Surgi-Aid Endoscopics, Inc.. The 510(k) number is K871809.

When did FLEXIBLE BIOPSY FORCEP receive FDA 510(k) clearance?

FLEXIBLE BIOPSY FORCEP received FDA 510(k) clearance on 1987-06-18, under 510(k) number K871809.

Who is the listed applicant for FLEXIBLE BIOPSY FORCEP?

The FDA 510(k) record lists Surgi-Aid Endoscopics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEXIBLE BIOPSY FORCEP?

The FDA product code for FLEXIBLE BIOPSY FORCEP is OCZ.

Related Clinical Trials

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.

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.

Official Source

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

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