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

Drain, Tee (Water Trap)

21 CFR 868.5995 / Anesthesiology
FDA source (opens on fda.gov)

BYH is the FDA product code for Drain, Tee (Water Trap), a class I device type, regulated under 21 CFR 868.5995. As of , FDA records hold 22 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
BYH
Device name
Drain, Tee (Water Trap)
Regulation
21 CFR 868.5995
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
22
Ingested recalls
2

Clearances, product code BYH

By decision year
22 clearances under product code BYH with a decision year between 1977 and 1995, 1990 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code BYH by decision year
YearClearances
19771
19792
19801
19811
19821
19841
19851
19863
19871
19882
19891
19904
19921
19931
19951

Applicants with the most clearances

Product code BYH
Applicants holding the most 510(k) clearances under product code BYH
ApplicantClearances
Dhd Medical Products Div. Diemolding Corp.5
Thayer Medical Corportation4
Airlife, Inc.2
Intertech Resources, Inc.2
Ballard Medical Products1
Carie Med-Tech Services, Inc.1
Hudson Oxygen Therapy Sales Co.1
Mem Medical, Inc.1
Ohio Medical Research, Inc.1
Pegasus Research Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 59 companies shown, in name order