MEDI-TECH DILATATION CATHETERS— 510(k) K844292

Substantially Equivalent

Medi-Tech, Inc.

FDA 510(k) clearance K844292 for MEDI-TECH DILATATION CATHETERS, Substantially Equivalent on 1984-11-23. Applicant: Medi-Tech, Inc.. Device class: 1.

Clearance details

Applicant: Medi-Tech, Inc.
Product code: Code LCN
Device class: Class 1
Regulation: 21 CFR 872.6855
Advisory panel: Dental
Date received: 1984-11-05
Decision date: 1984-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Watertown, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LCN

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K981808 — BREATHAID TONGUE SCRAPER1998-08-11

More clearances from Medi-Tech, Inc.

K954457 — MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER1996-05-15
K952345 — MEDI-TECH PLATFORM GUIDE CATHETER1995-08-17
K952056 — IMMUNOASSAY DRUGS OF ABUSE CONTROLS1995-06-01
K945289 — DOA - IMMUNOASSAY CUT-OFF CALIBRATOR1994-12-13
K942551 — THERAPEUTIC DRUG MONITORING CONTROL, ASSAYED1994-10-06

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