MEGA PARACENTESIS KIT— 510(k) K913382

Substantially Equivalent

Mega Medical, Inc.

FDA 510(k) clearance K913382 for MEGA PARACENTESIS KIT, Substantially Equivalent on 1991-10-08. Applicant: Mega Medical, Inc.. Device class: 2.

Clearance details

Applicant: Mega Medical, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1991-07-29
Decision date: 1991-10-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Mega Medical, Inc.

K915863 — MEGA AMNIOCENTESIS KIT1992-03-30
K913317 — MEGA ARTHROGRAM KIT1991-10-31
K913397 — MEGA ANGIOGRAM KIT1991-10-31
K912445 — MEGA CONTINUOUS EPIDURAL ANESTHESIA KIT1991-10-18
K912322 — MEGA SPINAL ANESTHESIA KIT1991-09-26

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