510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913397Unknown

Mega Angiogram Kit

Mega Medical, Inc., Tampa FL / Traditional, Unknown
FDA source (opens on fda.gov)

K913397 is the FDA 510(k) clearance record for MEGA ANGIOGRAM KIT, a class II device, cleared for Mega Medical, Inc. on under FDA product code DQO (Catheter, Intravascular, Diagnostic). FDA records list 7 510(k) clearances for Mega Medical, Inc., from to . As of , FDA records show no recalls naming K913397.

Clearance record

Decision date
Received
(93 days to decision)
Product code
DQO Catheter, Intravascular, Diagnostic
Regulation
21 CFR 870.1200
Device class
Class II
Review panel
Cardiovascular
Applicant
Mega Medical, Inc. P.O.Box 260956, Tampa FL
510(k) summary
Statement
Third party review
No

Clearances, product code DQO

Trailing 12 months
3 clearances under product code DQO in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DQO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20261
July 20260
August 20260
September 20260
October 20260