510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K922110Substantially Equivalent

Go-Clean

Viva-Tek Assoc., Inc., Medford NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K922110 is the FDA 510(k) clearance record for GO-CLEAN, a class II device, cleared for Viva-Tek Assoc., Inc. on under FDA product code FRR (Chamber, Reverse Isolation, Patient Care). FDA records list 2 510(k) clearances for Viva-Tek Assoc., Inc., from to . As of , FDA records show no recalls naming K922110.

Clearance record

Decision date
Received
(673 days to decision)
Product code
FRR Chamber, Reverse Isolation, Patient Care
Regulation
21 CFR 880.5450
Device class
Class II
Review panel
General Hospital
Applicant
Viva-Tek Assoc., Inc. 82 Chairville Rd., Medford NJ
510(k) summary
Statement
Third party review
No

Clearances, product code FRR

Trailing 12 months

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

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