510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883948Substantially Equivalent

Modified Numed Balloon Angiographic Catheter

Numed Inc, Hopkinton NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883948 is the FDA 510(k) clearance record for MODIFIED NUMED BALLOON ANGIOGRAPHIC CATHETER, a class II device, cleared for NuMED, Inc. on under FDA product code DYG (Catheter, Flow Directed). FDA records list 46 510(k) clearances for NuMED, Inc., from to . As of , FDA records show no recalls naming K883948.

Clearance record

Decision date
Received
(220 days to decision)
Product code
DYG Catheter, Flow Directed
Regulation
21 CFR 870.1240
Device class
Class II
Review panel
Cardiovascular
Applicant
NuMED, Inc. Main St., Hopkinton NY
Third party review
No

Clearances, product code DYG

Trailing 12 months

FDA records hold no clearances under product code DYG in the trailing twelve months.

FDA records show no clearances under product code DYG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DYG, 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 20260
October 20260