Cleared Traditional

K760908 - MINIATURE ASCENDING PAPER CHROMATO- (FDA 510(k) Clearance)

K760908 · Ackerman Nuclear, Inc. · Toxicology device

Nov 1976

Decision

24d

Days

Class 1

Risk

K760908 is an FDA 510(k) clearance for the MINIATURE ASCENDING PAPER CHROMATO-. This device is classified as a Apparatus, General Use, Thin Layer Chromatography (Class I - General Controls, product code DPA).

Submitted by Ackerman Nuclear, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 19, 1976, 24 days after receiving the submission on October 26, 1976.

This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.2270.

Submission Details

510(k) Number	K760908 FDA.gov
FDA Decision	Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received	October 26, 1976
Decision Date	November 19, 1976
Days to Decision	24 days
Submission Type	Traditional
Review Panel	Toxicology (TX)
Summary	—