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FDA 510(k)

GYN DISPOSABLES TENACULUM 356T

K-Number: K073182 · 2007-11-28

ApplicantGyn-Disposables, Inc.
Decision Date2007-11-28
Product CodeHDC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GYN DISPOSABLES TENACULUM 356T is the device name listed in this FDA 510(k) record. The listed applicant is Gyn-Disposables, Inc.. It received FDA 510(k) clearance on 2007-11-28 under 510(k) number K073182. The device is classified under product code HDC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GYN DISPOSABLES TENACULUM 356T?

GYN DISPOSABLES TENACULUM 356T is a medical device that received FDA 510(k) clearance on 2007-11-28. The listed applicant is Gyn-Disposables, Inc.. The 510(k) number is K073182.

When did GYN DISPOSABLES TENACULUM 356T receive FDA 510(k) clearance?

GYN DISPOSABLES TENACULUM 356T received FDA 510(k) clearance on 2007-11-28, under 510(k) number K073182.

Who is the listed applicant for GYN DISPOSABLES TENACULUM 356T?

The FDA 510(k) record lists Gyn-Disposables, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GYN DISPOSABLES TENACULUM 356T?

The FDA product code for GYN DISPOSABLES TENACULUM 356T is HDC.

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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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