510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K020896Substantially Equivalent

Oscor Pace 203/Pace 203H Dual-Chamber Temporary Pacemaker, St. Jude Medical, Model 3085 Dual-Chamber External Pulse Gene

Osypka Medical GmbH, La Jolla CA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K020896 is the FDA 510(k) clearance record for OSCOR PACE 203/PACE 203H DUAL-CHAMBER TEMPORARY PACEMAKER, ST. JUDE MEDICAL, MODEL 3085 DUAL-CHAMBER EXTERNAL PULSE GENE, a class II device, cleared for Osypka Medical, Inc. on under FDA product code DTE (Pulse-Generator, Pacemaker, External). FDA records list 7 510(k) clearances for Osypka Medical, Inc., from to . As of , FDA records show 2 recalls naming K020896.

Clearance record

Decision date
Received
(87 days to decision)
Product code
DTE Pulse-Generator, Pacemaker, External
Regulation
21 CFR 870.3600
Device class
Class II
Review panel
Cardiovascular
Applicant
Osypka Medical, Inc. 7463 Draper Ave., La Jolla CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DTE

Trailing 12 months

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

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