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FDA 510(k)

VANDERBILT CURETTE

K-Number: K761095 · 1976-11-30

ApplicantCodman & Shurtleff, Inc.
Decision Date1976-11-30
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VANDERBILT CURETTE 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 1976-11-30 under 510(k) number K761095. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANDERBILT CURETTE?

VANDERBILT CURETTE is a medical device that received FDA 510(k) clearance on 1976-11-30. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K761095.

When did VANDERBILT CURETTE receive FDA 510(k) clearance?

VANDERBILT CURETTE received FDA 510(k) clearance on 1976-11-30, under 510(k) number K761095.

Who is the listed applicant for VANDERBILT CURETTE?

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 VANDERBILT CURETTE?

The FDA product code for VANDERBILT CURETTE is HAO.

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Related Devices (Code: HAO)

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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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