510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802939Substantially Equivalent

Herpes Simplex Type I

Orion Diagnostica, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802939 is the FDA 510(k) clearance record for HERPES SIMPLEX TYPE I, a class II device, cleared for Orion Diagnostica, Inc. on under FDA product code GON (Antigen, Cf (Including Cf Control), Rubella). FDA records list 32 510(k) clearances for Orion Diagnostica, Inc., from to . As of , FDA records show no recalls naming K802939.

Clearance record

Decision date
Received
(42 days to decision)
Product code
GON Antigen, Cf (Including Cf Control), Rubella
Regulation
21 CFR 866.3510
Device class
Class II
Review panel
Microbiology
Applicant
Orion Diagnostica, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GON

Trailing 12 months

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

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