Cleared Traditional

K932496 - PRECISION MED PRODUCTS, LTD. BREATHING BAGS

K932496 is an FDA 510(k) clearance for PRECISION MED PRODUCTS, manufactured by Precision Med Products, Ltd.. The device is a Class 1 Anesthesiology device with product code BTC cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K932496 · Precision Med Products, Ltd. · Anesthesiology device
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Jul 1993
Decision
52d
Days
Class 1
Risk

K932496 is an FDA 510(k) clearance for the PRECISION MED PRODUCTS, LTD. BREATHING BAGS. Classified as Bag, Reservoir (product code BTC), Class I - General Controls.

Submitted by Precision Med Products, Ltd. (Marrtinsville, US). The FDA issued a Cleared decision on July 16, 1993 after a review of 52 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5320 - the FDA anesthesiology and respiratory 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 Precision Med Products, Ltd. devices

FDA 510(k) Submission Details - K932496

510(k) Number K932496 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 25, 1993
Decision Date July 16, 1993
Days to Decision 52 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 140d · This submission: 52d
Pathway characteristics
Predicate-based equivalence.

BTC Device Classification - Class 1, General Controls

Product Code BTC Bag, Reservoir
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5320
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 - BTC Bag, Reservoir

All 9
Devices cleared under the same product code (BTC) and FDA review panel - the closest regulatory comparables to K932496.
PeDIA
K181424 · Pedia, LLC · Sep 2018
BREATHING BAGS
K932581 · Med-Plastics Intl., Inc. · Jul 1993
BREATHING BAGS
K932584 · Merit Medical Systems, Inc. · Jul 1993
BREATHING BAGS
K932191 · Life Shield Healthcare Products, Inc. · Jul 1993
KING SYSTEMS, BREATHING BAG
K880680 · King Systems Corp. · Mar 1988
ANESTHESIA BREATHING BAG, VARIOUS SIZES
K822116 · Life Design Systems, Inc. · Aug 1982