FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BUSSE PLASTIC TUBING CONNECTORS AND ACCESSORIES

K Number: K935835 · Decision Jan 12, 1994
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
61
Applicant Total
31
Review Days
36

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Basic Information

Device Name
BUSSE PLASTIC TUBING CONNECTORS AND ACCESSORIES
K Number
K935835
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Busse Hospital Disposables, Inc.
Date Received
December 7, 1993
Decision Date
January 12, 1994
Product Code
BYX
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BYX Tubing, Pressure And Accessories

Similar 510(k) Clearances

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Other Clearances by Busse Hospital Disposables, Inc.

K Number Device Name
K120002 I-STYLE BONE MARROW ASPIRATION NEEDLE WITH T-HANDLE
K093909 BUSSE SURGICAL DRAPES IV
K092212 BUSSE SURGICAL DRAPES III
K082297 BUSSE SURGICAL DRAPE
K073222 MODIFICATION TO:SPECIALTY NEEDLES
K070465 BUSSE EPIDURAL CATHETER
K063018 GLASS LOSS OF RESISTANCE SYRINGE
K061394 SPECIALTY NEEDLES (SPINAL NEEDLE, PENCIL POINT SPINAL NEEDLE, EPIDURAL NEEDLE)
K061570 I-STYLE BONE MARROW ASPIRATION NEEDLE
K052843 BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE
Search all 31 clearances from Busse Hospital Disposables, Inc. →