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

DISPOSABLE BASE MOLD

K Number: K831335 · Decision May 16, 1983
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
4
Applicant Total
30
Review Days
21

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Basic Information

Device Name
DISPOSABLE BASE MOLD
K Number
K831335
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Surgipath Medical Industries, Inc.
Date Received
April 25, 1983
Decision Date
May 16, 1983
Product Code
KER
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
KER Container, Embedding

Similar 510(k) Clearances

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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. →