THIELER KIT— 510(k) K875153

Substantially Equivalent

Taris Corp.

FDA 510(k) clearance K875153 for THIELER KIT, Substantially Equivalent on 1988-02-18. Applicant: Taris Corp.. Device class: 2.

Clearance details

Applicant: Taris Corp.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1987-12-15
Decision date: 1988-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fernandina Beach, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Taris Corp.

K880887 — NEOCATH1988-05-24
K881256 — NON CORING INFUSION SET1988-04-21

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