TISSUE EMBEDDING MEDIUM— 510(k) K893772

Substantially Equivalent

Stephens Scientific

FDA 510(k) clearance K893772 for TISSUE EMBEDDING MEDIUM, Substantially Equivalent on 1989-06-22. Applicant: Stephens Scientific. Device class: 1.

Clearance details

Applicant: Stephens Scientific
Product code: Code KEO
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1989-05-22
Decision date: 1989-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denville, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KEO

K862223 — MICRO THIN* PARAFFIN1986-06-17
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 Stephens Scientific

K881359 — DECALCIFYING SOLUTION II1988-04-19
K872625 — DECALCIFYING SOLUTION1987-08-06
K832011 — AMERI CLEAR1983-08-12

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