510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K895956Substantially Equivalent

Rx02 Emergency Medical Oxygen

Progressive Medical Applications Corp., Allentown PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895956 is the FDA 510(k) clearance record for RX02 EMERGENCY MEDICAL OXYGEN, a class I device, cleared for Progressive Medical Applications Corp. on under FDA product code CAN (Regulator, Pressure, Gas Cylinder). FDA records list one 510(k) clearance for Progressive Medical Applications Corp. As of , FDA records show no recalls naming K895956.

Clearance record

Decision date
Received
(176 days to decision)
Product code
CAN Regulator, Pressure, Gas Cylinder
Regulation
21 CFR 868.2700
Device class
Class I
Review panel
Anesthesiology
Applicant
Progressive Medical Applications Corp. 1251 S. Cedar Crest Blvd., Allentown PA
Third party review
No

Clearances, product code CAN

Trailing 12 months

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

FDA records show no clearances under product code CAN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CAN, 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