510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K921757Substantially Equivalent

Angeion Igital Angeflator

Angeion Corp., Plymouth MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K921757 is the FDA 510(k) clearance record for ANGEION IGITAL ANGEFLATOR, a class II device, cleared for Angeion Corp. on under FDA product code MAV (Syringe, Balloon Inflation). FDA records list 7 510(k) clearances for Angeion Corp., from to . As of , FDA records show no recalls naming K921757.

Clearance record

Decision date
Received
(339 days to decision)
Product code
MAV Syringe, Balloon Inflation
Regulation
21 CFR 870.1650
Device class
Class II
Review panel
Cardiovascular
Applicant
Angeion Corp. 13000 Hwy. 55, Plymouth MN
510(k) summary
Statement
Third party review
No

Clearances, product code MAV

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