MEGA AMNIOCENTESIS KIT— 510(k) K915863

Unknown

Mega Medical, Inc.

FDA 510(k) clearance K915863 for MEGA AMNIOCENTESIS KIT, Unknown on 1992-03-30. Applicant: Mega Medical, Inc.. Device class: 1.

Clearance details

Applicant: Mega Medical, Inc.
Product code: Code HIO
Device class: Class 1
Regulation: 21 CFR 884.1550
Advisory panel: Obstetrics/Gynecology
Date received: 1991-12-31
Decision date: 1992-03-30
Decision: Unknown
Clearance type: Traditional
Location: Tampa, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HIO

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K955679 — RNS STERILE, DISPOSABLE AMNIOCENTESIS TRAY1996-03-12
K914419 — AMNIOTEST(TM)1993-09-01
K922960 — VARIOUS CAMEO MED AMNIOCENTESIS TRAYS, DISPOSABLE1992-11-05
K921738 — SONO-VU US(TM), MODIFICATION1992-04-27

More clearances from Mega Medical, Inc.

K913317 — MEGA ARTHROGRAM KIT1991-10-31
K913397 — MEGA ANGIOGRAM KIT1991-10-31
K912445 — MEGA CONTINUOUS EPIDURAL ANESTHESIA KIT1991-10-18
K913382 — MEGA PARACENTESIS KIT1991-10-08
K912322 — MEGA SPINAL ANESTHESIA KIT1991-09-26

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