510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770478Substantially Equivalent

Adapter, Cordis

Cordis US Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770478 is the FDA 510(k) clearance record for ADAPTER, CORDIS, a class II device, cleared for Cordis Corp. on under FDA product code DTD (Pacemaker Lead Adaptor). FDA records list 332 510(k) clearances for Cordis US Corp., from to . As of , FDA records show no recalls naming K770478.

Clearance record

Decision date
Received
(19 days to decision)
Product code
DTD Pacemaker Lead Adaptor
Regulation
21 CFR 870.3620
Device class
Class II
Review panel
Cardiovascular
Applicant
Cordis Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DTD

Trailing 12 months

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

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