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

SALINE SOLUTINE, STERILE

K Number: K950560 · Decision May 30, 1995
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
1
Applicant Total
31
Review Days
111

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Basic Information

Device Name
SALINE SOLUTINE, STERILE
K Number
K950560
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Busse Hospital Disposables, Inc.
Date Received
February 8, 1995
Decision Date
May 30, 1995
Product Code
IGE
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
IGE Solution, Formalin Ammonium Bromide

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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. →