Cleared Traditional

K900349 - PURITAN BENNETT SINGLE PATIENT USE PEEP...

K900349 is an FDA 510(k) clearance for PURITAN BENNETT SINGLE PATIENT USE PEEP..., manufactured by Puritan Bennett Corp.. The device is a Class 2 Anesthesiology device with product code BTM cleared through the Traditional 510(k) pathway after a 97-day FDA review.

K900349 · Puritan Bennett Corp. · Anesthesiology device
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May 1990
Decision
97d
Days
Class 2
Risk

K900349 is an FDA 510(k) clearance for the PURITAN BENNETT SINGLE PATIENT USE PEEP ADAPTER. Classified as Ventilator, Emergency, Manual (resuscitator) (product code BTM), Class II - Special Controls.

Submitted by Puritan Bennett Corp. (Overland Park, US). The FDA issued a Cleared decision on May 1, 1990 after a review of 97 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5915 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Puritan Bennett Corp. devices

FDA 510(k) Submission Details - K900349

510(k) Number K900349 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 24, 1990
Decision Date May 01, 1990
Days to Decision 97 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 140d · This submission: 97d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTM Device Classification - Class 2, Special Controls

Product Code BTM Ventilator, Emergency, Manual (resuscitator)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5915
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Anesthesiology devices follow this clearance model.

Regulatory Peers - BTM Ventilator, Emergency, Manual (resuscitator)

All 82
Devices cleared under the same product code (BTM) and FDA review panel - the closest regulatory comparables to K900349.
1ST RESPONSE REUSABLE MANUAL RESUSCITATOR (ADULT)
K900577 · Intertech Resources, Inc. · Jul 1990
AMBU SPUR (SINGLE PATIENT USE RESUSCITATOR) INFANT
K902261 · Ambu, Inc. · Jul 1990
AMBU LIFE KEY AND AMBU RES-CUE KEY
K900260 · Ambu, Inc. · Jun 1990
MANUAL RESUSCITATOR
K895589 · Hudson Oxygen Therapy Sales Co. · Mar 1990
RESPIRONICS INFANT BAGEASY
K895351 · Respironics, Inc. · Oct 1989
SINGLE PATIENT USE DISPOSABLE MANUAL RESUSCITATOR
K894365 · Puritan Bennett Corp. · Oct 1989