510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K862555Substantially Equivalent

Human Epitheloid Cervix Carcinoma Cells (Hela)

Viromed Laboratories, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862555 is the FDA 510(k) clearance record for HUMAN EPITHELOID CERVIX CARCINOMA CELLS (HELA), a class I device, cleared for Viromed Laboratories, Inc. on under FDA product code KIR (Cells, Animal And Human, Cultured). FDA records list 25 510(k) clearances for Viromed Laboratories, Inc., from to . As of , FDA records show no recalls naming K862555.

Clearance record

Decision date
Received
(7 days to decision)
Product code
KIR Cells, Animal And Human, Cultured
Regulation
21 CFR 864.2280
Device class
Class I
Review panel
Hematology
Applicant
Viromed Laboratories, Inc. 5100 Gamble Dr., Minneapolis MN
Third party review
No

Clearances, product code KIR

Trailing 12 months

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

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