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FDA 510(k)

BARD(R) DISPOSABLE BIOPSY FORCEPS

K-Number: K912549 · 1991-09-10

Decision Date1991-09-10
Product CodeFCL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD(R) DISPOSABLE BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1991-09-10 under 510(k) number K912549. The device is classified under product code FCL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD(R) DISPOSABLE BIOPSY FORCEPS?

BARD(R) DISPOSABLE BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1991-09-10. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K912549.

When did BARD(R) DISPOSABLE BIOPSY FORCEPS receive FDA 510(k) clearance?

BARD(R) DISPOSABLE BIOPSY FORCEPS received FDA 510(k) clearance on 1991-09-10, under 510(k) number K912549.

Who is the listed applicant for BARD(R) DISPOSABLE BIOPSY FORCEPS?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD(R) DISPOSABLE BIOPSY FORCEPS?

The FDA product code for BARD(R) DISPOSABLE BIOPSY FORCEPS is FCL.

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.

Other records listing C.R. Bard, Inc. as applicant

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.

View all 616 devices →

Related Devices (Code: FCL)

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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