EMBEDDING RINGS— 510(k) K831333

Name: FDA 510(k) clearance K831333
Creator: U.S. Food and Drug Administration
Published: 1983-05-25

Substantially Equivalent

Surgipath Medical Industries, Inc.

FDA 510(k) clearance K831333 for EMBEDDING RINGS, Substantially Equivalent on 1983-05-25. Applicant: Surgipath Medical Industries, Inc.. Device class: 1.

Clearance details

Applicant: Surgipath Medical Industries, Inc.
Product code: Code KER
Device class: Class 1
Regulation: 21 CFR 864.3010
Advisory panel: Pathology
Date received: 1983-04-25
Decision date: 1983-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KER

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K831922 — EMBEDDING RING1983-07-29
K831900 — MACLEAN-FOGG, DISP. BASE MOLD1983-07-28
K831335 — DISPOSABLE BASE MOLD1983-05-16
K772149 — LANCER BIOPSY HOLDER1977-11-22

More clearances from Surgipath Medical Industries, Inc.

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K883217 — SCHIFF REAGENT1988-08-05
K881921 — C-E BRUSH1988-07-19
K881922 — CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE1988-05-25
K881659 — TISSUE SECTION ADHESIVE1988-04-21
K863549 — REUSABLE/DISPOSABLE AUTOPSY KNIFE SET1986-09-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.