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

SED-FIX CONCENTRATE

K Number: K852045 · Decision Jun 10, 1985
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
0
Applicant Total
30
Review Days
32

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Basic Information

Device Name
SED-FIX CONCENTRATE
K Number
K852045
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Surgipath Medical Industries, Inc.
Date Received
May 9, 1985
Decision Date
June 10, 1985
Product Code
IER
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
IER Polyethylene Glycol (Carbowax)

Other Clearances by Surgipath Medical Industries, Inc.

K Number Device Name
K883217 SCHIFF REAGENT
K881921 C-E BRUSH
K881922 CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE
K881659 TISSUE SECTION ADHESIVE
K863549 REUSABLE/DISPOSABLE AUTOPSY KNIFE SET
K863616 KNIFE MAKER
K863548 ROTARY MICROTOME
K863483 CASSETTE EMBOSSEER
K863145 CERVICAL SCRAPERS
K861270 BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.
Search all 30 clearances from Surgipath Medical Industries, Inc. →