510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932480Substantially Equivalent

Prism

Bio Clinic Co., Ontario CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932480 is the FDA 510(k) clearance record for PRISM, a class II device, cleared for Bio Clinic Co. on under FDA product code IOQ (Bed, Flotation Therapy, Powered). FDA records list 14 510(k) clearances for Bio Clinic Co., from to . As of , FDA records show no recalls naming K932480.

Clearance record

Decision date
Received
(58 days to decision)
Product code
IOQ Bed, Flotation Therapy, Powered
Regulation
21 CFR 890.5170
Device class
Class II
Review panel
Physical Medicine
Applicant
Bio Clinic Co. 4083 E. Airport Dr., Ontario CA
510(k) summary
Summary
Third party review
No

Clearances, product code IOQ

Trailing 12 months

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

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