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
FQAClass I

Scale, Surgical Sponge

21 CFR 880.2740 / General Hospital
FDA source (opens on fda.gov)

FQA is the FDA product code for Scale, Surgical Sponge, a class I device type, regulated under 21 CFR 880.2740. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
FQA
Device name
Scale, Surgical Sponge
Regulation
21 CFR 880.2740
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
1

Clearances, product code FQA

By decision year
1 clearance under product code FQA with a decision year between 1983 and 1983, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FQA by decision year
YearClearances
19831

Applicants with the most clearances

Product code FQA
Applicants holding the most 510(k) clearances under product code FQA
ApplicantClearances
Ritmed, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 14 companies shown, in name order