510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K882833Substantially Equivalent

The Berg Resuscitation Apparatus

Hursch Ent., Inc., Greenville SC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K882833 is the FDA 510(k) clearance record for THE BERG RESUSCITATION APPARATUS, a class II device, cleared for Hursch Ent., Inc. on under FDA product code BTL (Ventilator, Emergency, Powered (Resuscitator)). FDA records list one 510(k) clearance for Hursch Ent., Inc. As of , FDA records show no recalls naming K882833.

Clearance record

Decision date
Received
(42 days to decision)
Product code
BTL Ventilator, Emergency, Powered (Resuscitator)
Regulation
21 CFR 868.5925
Device class
Class II
Review panel
Anesthesiology
Applicant
Hursch Ent., Inc. 2435 E. N. St., Suite, Greenville SC
Third party review
No

Clearances, product code BTL

Trailing 12 months

FDA records hold no clearances under product code BTL in the trailing twelve months.

FDA records show no clearances under product code BTL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BTL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260