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

Gauze/Sponge, Internal

Unknown
FDA source (opens on fda.gov)

EFQ is the FDA product code for Gauze/Sponge, Internal. As of , FDA records hold 271 510(k) clearances under this code, the most recent dated , and 13 recalls.

Classification record

Product code
EFQ
Device name
Gauze/Sponge, Internal
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
271
Ingested recalls
13

Clearances, product code EFQ

By decision year
271 clearances under product code EFQ with a decision year between 1976 and 1999, 1994 the highest year at 49.
Show the numbers
510(k) clearances under FDA product code EFQ by decision year
YearClearances
19762
19775
19785
19796
198023
19817
19827
198318
19843
198514
198618
198717
198822
198911
19901
19914
19923
19932
199449
199516
199616
199710
19986
19996

Applicants with the most clearances

Product code EFQ
Applicants holding the most 510(k) clearances under product code EFQ
ApplicantClearances
McNeil Healthcare LLC14
Ormed Mfg., Inc.14
American Medical Disposable, Inc.13
Ritmed, Inc.10
Certified Safety Mfg Inc8
Fraass Survival Systems, Inc.8
Applied Medical6
Lorons International Corp.6
Lorrex Health Products6
Abco Dealers, Inc.5

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 45 companies shown, in name order