Cleared Traditional

K772075 - RADIAL IMMUNODIFFUSION KIT-COMPLEMENT
(FDA 510(k) Clearance)

K772075 · Gelman Instrument Co. · Immunology
Feb 1978
Decision
92d
Days
Class 2
Risk

K772075 is an FDA 510(k) clearance for the RADIAL IMMUNODIFFUSION KIT-COMPLEMENT. This device is classified as a Complement C5, Antigen, Antiserum, Control (Class II — Special Controls, product code DAY).

Submitted by Gelman Instrument Co. (Mchenry, US). The FDA issued a Cleared decision on February 3, 1978, 92 days after receiving the submission on November 3, 1977.

This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5240.

Submission Details

510(k) Number K772075 FDA.gov
FDA Decision Cleared SESE
Date Received November 03, 1977
Decision Date February 03, 1978
Days to Decision 92 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary —

Device Classification

Product Code DAY — Complement C5, Antigen, Antiserum, Control
Device Class Class II — Special Controls
CFR Regulation 21 CFR 866.5240