Cleared Traditional

K882833 - THE BERG RESUSCITATION APPARATUS

K882833 is an FDA 510(k) clearance for THE BERG RESUSCITATION APPARATUS, manufactured by Hursch Ent., Inc.. The device is a Class 2 Anesthesiology device with product code BTL cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K882833 · Hursch Ent., Inc. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1988
Decision
42d
Days
Class 2
Risk

K882833 is an FDA 510(k) clearance for the THE BERG RESUSCITATION APPARATUS. Classified as Ventilator, Emergency, Powered (resuscitator) (product code BTL), Class II - Special Controls.

Submitted by Hursch Ent., Inc. (Greenville, US). The FDA issued a Cleared decision on August 19, 1988 after a review of 42 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5925 - 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.

FDA 510(k) Submission Details - K882833

510(k) Number K882833 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 08, 1988
Decision Date August 19, 1988
Days to Decision 42 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
98d faster than avg
Panel avg: 140d · This submission: 42d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTL Device Classification - Class 2, Special Controls

Product Code BTL Ventilator, Emergency, Powered (resuscitator)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5925
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 - BTL Ventilator, Emergency, Powered (resuscitator)

All 83
Devices cleared under the same product code (BTL) and FDA review panel - the closest regulatory comparables to K882833.
OHMEDA - LOGIC 07A TRANSPORT VENTILATOR
K901846 · Ohmeda Medical · Aug 1990
BIVONA CARDEN INTERMITTENT JETTING DEVICE
K895946 · Bivona Medical Technologies · Jan 1990
RESUBMITTED RD1000 NEOPUFF INFANT RESUSCITATOR
K892885 · Fisher & Paykel Electronics , Ltd. · Oct 1989
LSP AUTOMATIC VENTILATOR, MODEL 456
K870424 · Life Support Products, Inc. · Jan 1988
AUTOMATIC VENTILATOR AV2000
K874656 · Life Support Products, Inc. · Jan 1988
PATIENT VALVE WITH AIR ENTRAINMENT
K863410 · Pneupac , Ltd. · Jan 1987
K882833 · THE BERG RESUSCITATION APPARATUS
Download PDF Hursch Ent., Inc.