510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K981203Substantially Equivalent

Rusch Blakemore 3 Lumen, Sterile

Rusch Intl., Jeffrey NH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K981203 is the FDA 510(k) clearance record for RUSCH BLAKEMORE 3 LUMEN, STERILE, a class II device, cleared for Rusch Intl. on under FDA product code KNT (Tubes, Gastrointestinal (And Accessories)). FDA records list 43 510(k) clearances for Rusch Intl., from to . As of , FDA records show one recall naming K981203.

Clearance record

Decision date
Received
(64 days to decision)
Product code
KNT Tubes, Gastrointestinal (And Accessories)
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Rusch Intl. Tall Pines Park, Jeffrey NH
510(k) summary
Summary
Third party review
No

Clearances, product code KNT

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