510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K980052Substantially Equivalent

Respaide

Emergency Filtration Products, Inc., St. George UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980052 is the FDA 510(k) clearance record for RESPAIDE, a class II device, cleared for Emergency Filtration Products, Inc. on under FDA product code CBP (Valve, Non-Rebreathing). FDA records list 2 510(k) clearances for Emergency Filtration Products, Inc., from to . As of , FDA records show no recalls naming K980052.

Clearance record

Decision date
Received
(211 days to decision)
Product code
CBP Valve, Non-Rebreathing
Regulation
21 CFR 868.5870
Device class
Class II
Review panel
Anesthesiology
Applicant
Emergency Filtration Products, Inc. 321 N. Mall Dr., St. George UT
510(k) summary
Summary
Third party review
No

Clearances, product code CBP

Trailing 12 months

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

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