510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
BYYClass II

Tube, Aspirating, Flexible, Connecting

21 CFR 880.6740 / General Hospital
FDA source (opens on fda.gov)

BYY is the FDA product code for Tube, Aspirating, Flexible, Connecting, a class II device type, regulated under 21 CFR 880.6740. As of , FDA records hold 24 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
BYY
Device name
Tube, Aspirating, Flexible, Connecting
Regulation
21 CFR 880.6740
Device class
Class II
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
24
Ingested recalls
6

Clearances, product code BYY

By decision year
24 clearances under product code BYY with a decision year between 1976 and 1996, 1996 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code BYY by decision year
YearClearances
19761
19781
19792
19801
19812
19823
19833
19841
19851
19871
19901
19911
19941
19965

Applicants with the most clearances

Product code BYY
Applicants holding the most 510(k) clearances under product code BYY
ApplicantClearances
Bio-Medical Devices, Inc.3
American Pharmaseal Div. Ahsc2
Mgn Medical Manufacturing, Inc.2
Snyder Laboratories, Inc.2
Abco Dealers, Inc.1
Acacia Laboratories, Inc.1
Custom Pack Reliability1
Davol, Inc.1
MEDLINE INDUSTRIES, LP - Northfield1
Megadyne Medical Products, Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 152 companies shown, in name order