Cleared Traditional

K962739 - T.B.Q.

K962739 is the FDA 510(k) clearance for T.B.Q. by Convatec, A Division of E.R. Squibb & Sons. It is a Class 1 General Hospital device (product code LRJ) cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K962739 · Convatec, A Division of E.R. Squibb & Sons · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1996
Decision
84d
Days
Class 1
Risk

K962739 is an FDA 510(k) clearance for the T.B.Q.. Classified as Disinfectant, Medical Devices (product code LRJ), Class I - General Controls.

Submitted by Convatec, A Division of E.R. Squibb & Sons (Princeton, US). The FDA issued a Cleared decision on October 7, 1996 after a review of 84 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6890 - the FDA general hospital 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Convatec, A Division of E.R. Squibb & Sons devices

Submission Details

510(k) Number K962739 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 15, 1996
Decision Date October 07, 1996
Days to Decision 84 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
45d faster than avg
Panel avg: 129d · This submission: 84d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LRJ Disinfectant, Medical Devices
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6890
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 - LRJ Disinfectant, Medical Devices

All 11
Devices cleared under the same product code (LRJ) and FDA review panel - the closest regulatory comparables to K962739.
GERMICIDAL CLOTH
K974304 · Convatec, A Division of E.R. Squibb & Sons · Jan 1998
COVERAGE SPRAY HBV
K964835 · Convatec, A Division of E.R. Squibb & Sons · Dec 1996
COVERAGE HBV
K964749 · Convatec, A Division of E.R. Squibb & Sons · Dec 1996
VACUSOL PLUS DENTAL VACUUM LINE CLEANER/DISINFECTANT
K934014 · Biotrol, USA, Inc. · Dec 1995
RENALIN COLD STERILANT
K941439 · Minntech Corp. · Jun 1995
CIDEX PLUS 28 DAY SOLUTION
K923744 · Johnson & Johnson Medical, Inc. · Mar 1994