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
GGQClass II

Test, Prothrombin Consumption

21 CFR 864.7720 / Hematology
FDA source (opens on fda.gov)

GGQ is the FDA product code for Test, Prothrombin Consumption, a class II device type, regulated under 21 CFR 864.7720. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GGQ
Device name
Test, Prothrombin Consumption
Regulation
21 CFR 864.7720
Device class
Class II
Review panel
Hematology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code GGQ

By decision year
2 clearances under product code GGQ with a decision year between 1980 and 1981, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code GGQ by decision year
YearClearances
19801
19811

Applicants with the most clearances

Product code GGQ
Applicants holding the most 510(k) clearances under product code GGQ
ApplicantClearances
Abbott Medical2

Companies listing this code with FDA

Companies whose registered establishments list this code