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

Absorber, Carbon-Dioxide

21 CFR 868.5310 / Anesthesiology
FDA source (opens on fda.gov)

BSF is the FDA product code for Absorber, Carbon-Dioxide, a class I device type, regulated under 21 CFR 868.5310. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
BSF
Device name
Absorber, Carbon-Dioxide
Regulation
21 CFR 868.5310
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
8
Ingested recalls
6

Clearances, product code BSF

By decision year
8 clearances under product code BSF with a decision year between 1976 and 1995, 1984 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code BSF by decision year
YearClearances
19761
19801
19821
19831
19842
19851
19951

Applicants with the most clearances

Product code BSF
Applicants holding the most 510(k) clearances under product code BSF
ApplicantClearances
GE Healthcare2
Airco/Ohio Medical Products1
Fraser Sweatman, Inc.1
G & L Unltd.1
King Systems Corporation.1
Ohio Medical Products1
Penlon, Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 23 companies shown, in name order