Las-R Human Alpha, Antitrypsin Test

FDA 510(k) K760916 · Hyland Therapeutic Div., Travenol Laboratories

Substantially Equivalent

510(k) numberK760916

Submission

Device name
Las-R Human Alpha, Antitrypsin Test
Applicant
Hyland Therapeutic Div., Travenol Laboratories
Mchenry, IL, US
Received
October 28, 1976
Decision date
November 16, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DEM – Alpha-1-Antitrypsin, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5130
Specialty
Immunology

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Questions and answers

When was Las-R Human Alpha, Antitrypsin Test cleared by the FDA?

Las-R Human Alpha, Antitrypsin Test (K760916) received a 510(k) decision of Substantially Equivalent on November 16, 1976, 19 days after the submission was received.

What is the product code of K760916?

The FDA product code is DEM – Alpha-1-Antitrypsin, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5130.