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FDA 510(k)

DAWN DISPOSABLE BIOPSY FORCEPS

K-Number: K933135 · 1994-03-07

ApplicantDawn Medical
Decision Date1994-03-07
Product CodeFCL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAWN DISPOSABLE BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Dawn Medical. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K933135. 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 DAWN DISPOSABLE BIOPSY FORCEPS?

DAWN DISPOSABLE BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Dawn Medical. The 510(k) number is K933135.

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

DAWN DISPOSABLE BIOPSY FORCEPS received FDA 510(k) clearance on 1994-03-07, under 510(k) number K933135.

Who is the listed applicant for DAWN DISPOSABLE BIOPSY FORCEPS?

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

What is the FDA product code for DAWN DISPOSABLE BIOPSY FORCEPS?

The FDA product code for DAWN 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 Dawn Medical 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.

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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