MICRO THIN* PARAFFIN— 510(k) K862223

Name: FDA 510(k) clearance K862223
Creator: U.S. Food and Drug Administration
Published: 1986-06-17

Substantially Equivalent

Richard-Allan Medical Ind., Inc.

FDA 510(k) clearance K862223 for MICRO THIN* PARAFFIN, Substantially Equivalent on 1986-06-17. Applicant: Richard-Allan Medical Ind., Inc.. Device class: 1.

Clearance details

Applicant: Richard-Allan Medical Ind., Inc.
Product code: Code KEO
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1986-06-11
Decision date: 1986-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richland, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KEO

view all

K893772 — TISSUE EMBEDDING MEDIUM1989-06-22
K862141 — HISTOLOGY PARAFFIN1986-06-13
K861270 — BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.1986-04-11
K842053 — PARAPLAST EXTRA TISSUE EMBEDDING MED.1984-06-26
K833071 — TECHNICON PARACUT1983-10-14

More clearances from Richard-Allan Medical Ind., Inc.

view all

K931879 — REFLEX HTR1994-03-24
K924200 — REFLEX(R) ESC1994-02-22
K926297 — REFLEX ESI1993-10-15
K924761 — STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELD1993-04-20
K900566 — RICHARD-ALLAN VESSEL LOOPS1990-05-03

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