FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE

K Number: K874306 · Decision Mar 22, 1988
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
11
Applicant Total
31
Review Days
154

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Basic Information

Device Name
INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE
K Number
K874306
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5450
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Busse Hospital Disposables, Inc.
Date Received
October 20, 1987
Decision Date
March 22, 1988
Product Code
LGM
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LGM Chamber, Patient Isolation

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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. →