510(k) K833307

PHADEBACK G.C. POSITIVE CONTROLS by Pharmacia, Inc. — Product Code JSX

K833307 is an FDA 510(k) premarket notification submitted by Pharmacia, Inc. for the device "PHADEBACK G.C. POSITIVE CONTROLS". The FDA issued a decision of Substantially Equivalent on December 27, 1983. The device falls under product code JSX (Kit, Identification, Neisseria Gonorrhoeae), a Class I device regulated under 21 CFR 866.2660. Pharmacia, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 27, 1983
Date Received
September 23, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Identification, Neisseria Gonorrhoeae
Device Class
Class I
Regulation Number
866.2660
Review Panel
MI
Submission Type