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FDA 510(k)

CODMAN LHALO SPLIT RING RETRACTOR SYSTEM

K-Number: K913233 · 1991-07-31

ApplicantCodman & Shurtleff, Inc.
Decision Date1991-07-31
Product CodeGZT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN LHALO SPLIT RING RETRACTOR SYSTEM 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 1991-07-31 under 510(k) number K913233. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN LHALO SPLIT RING RETRACTOR SYSTEM?

CODMAN LHALO SPLIT RING RETRACTOR SYSTEM is a medical device that received FDA 510(k) clearance on 1991-07-31. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K913233.

When did CODMAN LHALO SPLIT RING RETRACTOR SYSTEM receive FDA 510(k) clearance?

CODMAN LHALO SPLIT RING RETRACTOR SYSTEM received FDA 510(k) clearance on 1991-07-31, under 510(k) number K913233.

Who is the listed applicant for CODMAN LHALO SPLIT RING RETRACTOR SYSTEM?

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 LHALO SPLIT RING RETRACTOR SYSTEM?

The FDA product code for CODMAN LHALO SPLIT RING RETRACTOR SYSTEM is GZT.

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Related Devices (Code: GZT)

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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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