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FDA 510(k)

BRIMFIELD CANNULATED GRASPING HOOKS

K-Number: K843136 · 1984-09-25

Decision Date1984-09-25
Product CodeGDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BRIMFIELD CANNULATED GRASPING HOOKS is the device name listed in this FDA 510(k) record. The listed applicant is Brimfield Scientific Instruments. It received FDA 510(k) clearance on 1984-09-25 under 510(k) number K843136. The device is classified under product code GDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRIMFIELD CANNULATED GRASPING HOOKS?

BRIMFIELD CANNULATED GRASPING HOOKS is a medical device that received FDA 510(k) clearance on 1984-09-25. The listed applicant is Brimfield Scientific Instruments. The 510(k) number is K843136.

When did BRIMFIELD CANNULATED GRASPING HOOKS receive FDA 510(k) clearance?

BRIMFIELD CANNULATED GRASPING HOOKS received FDA 510(k) clearance on 1984-09-25, under 510(k) number K843136.

Who is the listed applicant for BRIMFIELD CANNULATED GRASPING HOOKS?

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

What is the FDA product code for BRIMFIELD CANNULATED GRASPING HOOKS?

The FDA product code for BRIMFIELD CANNULATED GRASPING HOOKS is GDG.

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 Brimfield Scientific Instruments 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: GDG)

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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