510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K884004Substantially Equivalent

Rubeola Test

Gull Laboratories, Inc., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884004 is the FDA 510(k) clearance record for RUBEOLA TEST, a class I device, cleared for Gull Laboratories, Inc. on under FDA product code GRE (Antiserum, Fluorescent, Rubeola). FDA records list 57 510(k) clearances for Gull Laboratories, Inc., from to . As of , FDA records show no recalls naming K884004.

Clearance record

Decision date
Received
(75 days to decision)
Product code
GRE Antiserum, Fluorescent, Rubeola
Regulation
21 CFR 866.3520
Device class
Class I
Review panel
Microbiology
Applicant
Gull Laboratories, Inc. 1011 E. 4800 S., Salt Lake City UT
Third party review
No

Clearances, product code GRE

Trailing 12 months

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

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