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

Cabinet, Table And Tray, Anesthesia

21 CFR 868.6100 / Anesthesiology
FDA source (opens on fda.gov)

BRY is the FDA product code for Cabinet, Table And Tray, Anesthesia, a class I device type, regulated under 21 CFR 868.6100. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and 99 recalls.

Classification record

Product code
BRY
Device name
Cabinet, Table And Tray, Anesthesia
Regulation
21 CFR 868.6100
Device class
Class I
Review panel
Anesthesiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
99

Clearances, product code BRY

By decision year
5 clearances under product code BRY with a decision year between 1982 and 1992, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code BRY by decision year
YearClearances
19821
19871
19901
19911
19921

Applicants with the most clearances

Product code BRY
Applicants holding the most 510(k) clearances under product code BRY
ApplicantClearances
Anestech, Inc.1
John J. Navar, M.D.1
Med-Life, Inc.1
Medikeeper, Inc.1
Siemens Life Support Systems1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 56 companies shown, in name order