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FDA 510(k)

DISPOSABLE PERFORATOR

K-Number: K924242 · 1993-07-08

ApplicantCodman & Shurtleff, Inc.
Decision Date1993-07-08
Product CodeHBF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PERFORATOR 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 1993-07-08 under 510(k) number K924242. 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 PERFORATOR?

DISPOSABLE PERFORATOR is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K924242.

When did DISPOSABLE PERFORATOR receive FDA 510(k) clearance?

DISPOSABLE PERFORATOR received FDA 510(k) clearance on 1993-07-08, under 510(k) number K924242.

Who is the listed applicant for DISPOSABLE PERFORATOR?

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 PERFORATOR?

The FDA product code for DISPOSABLE PERFORATOR is HBF.

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Official Source

View on FDA Database →

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

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