Cleared Traditional

TISSUE CULTURE TUBES

K873889 · Nunc, Inc. · Pathology

Nov 1987

Decision

63d

Days

Class 1

Risk

About This 510(k) Submission

K873889 is an FDA 510(k) clearance for the TISSUE CULTURE TUBES, a Flask, Tissue Culture (Class I — General Controls, product code KJA), submitted by Nunc, Inc. (Riverside, US). The FDA issued a Cleared decision on November 25, 1987, 63 days after receiving the submission on September 23, 1987. This device falls under the Pathology review panel. Regulated under 21 CFR 864.2240.

Submission Details

510(k) Number	K873889 FDA.gov
FDA Decision	Cleared SESE
Date Received	September 23, 1987
Decision Date	November 25, 1987
Days to Decision	63 days
Submission Type	Traditional
Review Panel	Pathology (PA)
Summary	—