Pre-Cut Tracheostomy Dressing Sterile, Disposable

FDA 510(k) K920282 · Trinity Laboratories, Inc.

Substantially Equivalent

510(k) numberK920282

Submission

Device name
Pre-Cut Tracheostomy Dressing Sterile, Disposable
Applicant
Trinity Laboratories, Inc.
Salisbury, MD, US
Received
January 22, 1992
Decision date
May 29, 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
NAB – Gauze / Sponge,Nonresorbable For External Use
Device class
Class I (low risk)
Regulation
21 CFR 878.4014
Specialty
General, Plastic Surgery

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Questions and answers

When was Pre-Cut Tracheostomy Dressing Sterile, Disposable cleared by the FDA?

Pre-Cut Tracheostomy Dressing Sterile, Disposable (K920282) received a 510(k) decision of Substantially Equivalent on May 29, 1992, 128 days after the submission was received.

What is the product code of K920282?

The FDA product code is NAB – Gauze / Sponge,Nonresorbable For External Use, a Class I (low risk) device regulated under 21 CFR 878.4014.