Triangular Jaw Microlaryngeal Forceps

FDA 510(k) K925370 · Pilling Co.

Substantially Equivalent

510(k) numberK925370

Submission

Device name
Triangular Jaw Microlaryngeal Forceps
Applicant
Pilling Co.
Fort Washington, PA, US
Received
October 23, 1992
Decision date
March 18, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
ELW – Material, Impression
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3660
Specialty
Dental

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Questions and answers

When was Triangular Jaw Microlaryngeal Forceps cleared by the FDA?

Triangular Jaw Microlaryngeal Forceps (K925370) received a 510(k) decision of Substantially Equivalent on March 18, 1993, 146 days after the submission was received.

What is the product code of K925370?

The FDA product code is ELW – Material, Impression, a Class II (moderate risk) device regulated under 21 CFR 872.3660.