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FDA 510(k)

DISPOSABLE PERFORATORS, JACOBS, HUDSON

K-Number: K791101 · 1979-08-28

ApplicantCodman & Shurtleff, Inc.
Decision Date1979-08-28
Product CodeHBF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PERFORATORS, JACOBS, HUDSON is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1979-08-28 under 510(k) number K791101. The device is classified under product code HBF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE PERFORATORS, JACOBS, HUDSON?

DISPOSABLE PERFORATORS, JACOBS, HUDSON is a medical device that received FDA 510(k) clearance on 1979-08-28. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K791101.

When did DISPOSABLE PERFORATORS, JACOBS, HUDSON receive FDA 510(k) clearance?

DISPOSABLE PERFORATORS, JACOBS, HUDSON received FDA 510(k) clearance on 1979-08-28, under 510(k) number K791101.

Who is the listed applicant for DISPOSABLE PERFORATORS, JACOBS, HUDSON?

The FDA 510(k) record lists Codman & Shurtleff, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE PERFORATORS, JACOBS, HUDSON?

The FDA product code for DISPOSABLE PERFORATORS, JACOBS, HUDSON is HBF.

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Related Devices (Code: HBF)

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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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