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FDA 510(k)

CODMAN SUCTION PUNCH-PRODUCT CODES

K-Number: K842774 · 1984-07-27

ApplicantCodman & Shurtleff, Inc.
Decision Date1984-07-27
Product CodeHTZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CODMAN SUCTION PUNCH-PRODUCT CODES 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 1984-07-27 under 510(k) number K842774. The device is classified under product code HTZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN SUCTION PUNCH-PRODUCT CODES?

CODMAN SUCTION PUNCH-PRODUCT CODES is a medical device that received FDA 510(k) clearance on 1984-07-27. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K842774.

When did CODMAN SUCTION PUNCH-PRODUCT CODES receive FDA 510(k) clearance?

CODMAN SUCTION PUNCH-PRODUCT CODES received FDA 510(k) clearance on 1984-07-27, under 510(k) number K842774.

Who is the listed applicant for CODMAN SUCTION PUNCH-PRODUCT CODES?

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 CODMAN SUCTION PUNCH-PRODUCT CODES?

The FDA product code for CODMAN SUCTION PUNCH-PRODUCT CODES is HTZ.

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Related Devices (Code: HTZ)

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.

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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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