Cleared Traditional

K833307 - PHADEBACK G.C. POSITIVE CONTROLS

K833307 is the FDA 510(k) clearance for PHADEBACK G.C. POSITIVE CONTROLS by Pharmacia, Inc.. It is a Class 1 Microbiology device (product code JSX) cleared through the Traditional 510(k) pathway after a 95-day FDA review.

K833307 · Pharmacia, Inc. · Microbiology device
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Dec 1983
Decision
95d
Days
Class 1
Risk

K833307 is an FDA 510(k) clearance for the PHADEBACK G.C. POSITIVE CONTROLS. Classified as Kit, Identification, Neisseria Gonorrhoeae (product code JSX), Class I - General Controls.

Submitted by Pharmacia, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 27, 1983 after a review of 95 days - within the typical 510(k) review window.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2660 - the FDA microbiology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Pharmacia, Inc. devices

Submission Details

510(k) Number K833307 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 1983
Decision Date December 27, 1983
Days to Decision 95 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
7d faster than avg
Panel avg: 102d · This submission: 95d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSX Kit, Identification, Neisseria Gonorrhoeae
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2660
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - JSX Kit, Identification, Neisseria Gonorrhoeae

Devices cleared under the same product code (JSX) and FDA review panel - the closest regulatory comparables to K833307.
NIZYME TEST KIT
K923566 · Remel Co. · Nov 1992
XACT NEISSERIA
K880511 · Austin Biological Laboratories · Aug 1988
QUAD FERM +
K853544 · Analytical Products, Inc. · Sep 1985
NEISSERIA IDENTIFICATION DISCS
K830364 · Oxoid U.S.A., Inc. · Mar 1983
GONO-CELL
K782013 · Abbott Laboratories · Apr 1979
MICROCULT-GC CULTURE TEST
K781108 · Miles Laboratories, Inc. · Aug 1978