510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K974868Substantially Equivalent

Sigma Plus Monoplace Hyperbaric Chamber

Perry Baromedical Corporation, Riviera Beach FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974868 is the FDA 510(k) clearance record for SIGMA PLUS MONOPLACE HYPERBARIC CHAMBER, a class II device, cleared for Perry Baromedical Corp. on under FDA product code CBF (Chamber, Hyperbaric). FDA records list 3 510(k) clearances for Perry Baromedical Corp., from to . As of , FDA records show no recalls naming K974868.

Clearance record

Decision date
Received
(185 days to decision)
Product code
CBF Chamber, Hyperbaric
Regulation
21 CFR 868.5470
Device class
Class II
Review panel
Anesthesiology
Applicant
Perry Baromedical Corp. 7555 Garden Rd., Riviera Beach FL
510(k) summary
Summary
Third party review
No

Clearances, product code CBF

Trailing 12 months

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

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