TECHNICON PARACUT— 510(k) K833071

Substantially Equivalent

Technicon Instruments Corp.

FDA 510(k) clearance K833071 for TECHNICON PARACUT, Substantially Equivalent on 1983-10-14. Applicant: Technicon Instruments Corp.. Device class: 1.

Clearance details

Applicant: Technicon Instruments Corp.
Product code: Code KEO
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1983-09-08
Decision date: 1983-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KEO

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K862141 — HISTOLOGY PARAFFIN1986-06-13
K861270 — BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.1986-04-11
K842053 — PARAPLAST EXTRA TISSUE EMBEDDING MED.1984-06-26

More clearances from Technicon Instruments Corp.

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K914025 — TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)1991-11-22
K912616 — TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES1991-09-25
K912413 — CHEM-LINK DATA BASE MANAGER1991-07-01

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