510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K973373Substantially Equivalent

Prevent I

The Buzzz Corp., Larksville PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973373 is the FDA 510(k) clearance record for PREVENT I, a class II device, cleared for The Buzzz Corp. on under FDA product code INO (Chair, Positioning, Electric). FDA records list 4 510(k) clearances for The Buzzz Corp., from to . As of , FDA records show no recalls naming K973373.

Clearance record

Decision date
Received
(171 days to decision)
Product code
INO Chair, Positioning, Electric
Regulation
21 CFR 890.3110
Device class
Class II
Review panel
Physical Medicine
Applicant
The Buzzz Corp. 213 E. Luzerne Ave., Larksville PA
510(k) summary
Statement
Third party review
No

Clearances, product code INO

Trailing 12 months

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

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