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

Spreader, Cuff

21 CFR 868.5760 / Anesthesiology
FDA source (opens on fda.gov)

CBG is the FDA product code for Spreader, Cuff, a class I device type, regulated under 21 CFR 868.5760. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
CBG
Device name
Spreader, Cuff
Regulation
21 CFR 868.5760
Device class
Class I
Review panel
Anesthesiology
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
0

Clearances, product code CBG

By decision year
1 clearance under product code CBG with a decision year between 1987 and 1987, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CBG by decision year
YearClearances
19871

Applicants with the most clearances

Product code CBG
Applicants holding the most 510(k) clearances under product code CBG
ApplicantClearances
Kalajian Ent.1

Companies listing this code with FDA

Companies whose registered establishments list this code