510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K871615Substantially Equivalent

U. V. Germicidal Unit

Lorvic Corp., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871615 is the FDA 510(k) clearance record for U. V. GERMICIDAL UNIT, a class II device, cleared for Lorvic Corp. on under FDA product code KMH (Sterilizer, Dry Heat). FDA records list 6 510(k) clearances for Lorvic Corp., from to . As of , FDA records show no recalls naming K871615.

Clearance record

Decision date
Received
(137 days to decision)
Product code
KMH Sterilizer, Dry Heat
Regulation
21 CFR 880.6870
Device class
Class II
Review panel
General Hospital
Applicant
Lorvic Corp. 8810 Frost Ave., St. Louis MO
Third party review
No

Clearances, product code KMH

Trailing 12 months

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

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