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

Scale, Sponge, Surgical, Electrically-Powered

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

MRL is the FDA product code for Scale, Sponge, Surgical, Electrically-Powered, 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 no recalls.

Classification record

Product code
MRL
Device name
Scale, Sponge, Surgical, Electrically-Powered
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
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code MRL

By decision year
1 clearance under product code MRL with a decision year between 1997 and 1997, 1997 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MRL by decision year
YearClearances
19971

Applicants with the most clearances

Product code MRL
Applicants holding the most 510(k) clearances under product code MRL
ApplicantClearances
Surgitrac Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code