General Surgery Clamp and Needle Holder

FDA 510(k) K922659 · Miltex Instrument Co.

Substantially Equivalent

510(k) numberK922659

Submission

Device name
General Surgery Clamp and Needle Holder
Applicant
Miltex Instrument Co.
Lake Success, NY, US
Received
June 3, 1992
Decision date
July 21, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GDJ – Clamp, Surgical, General & Plastic Surgery
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

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K895726Vessel OccluderGDJ · Traditional Applied Medical Technologies10/24/1989SE
K895591Silicone Instrument ShodsGDJ · Traditional Key Surgical, Inc.10/20/1989SE
K882169Surgical Duct Clamp (Vine)GDJ · Traditional Henley Intl.06/17/1988SE
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Questions and answers

When was General Surgery Clamp and Needle Holder cleared by the FDA?

General Surgery Clamp and Needle Holder (K922659) received a 510(k) decision of Substantially Equivalent on July 21, 1992, 48 days after the submission was received.

What is the product code of K922659?

The FDA product code is GDJ – Clamp, Surgical, General & Plastic Surgery, a Class I (low risk) device regulated under 21 CFR 878.4800.