FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIPOLAR TEMP. PACING CATHETER W/STYLETET

K Number: K822002 · Decision Oct 15, 1982
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
128
Applicant Total
16
Review Days
99

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BIPOLAR TEMP. PACING CATHETER W/STYLETET
K Number
K822002
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Ziehm International, Inc.
Date Received
July 8, 1982
Decision Date
October 15, 1982
Product Code
LDF
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LDF Electrode, Pacemaker, Temporary

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LDF), ordered by most recent decision date.

View all

Other Clearances by Ziehm International, Inc.

K Number Device Name
K011292 ZIEHM VISION
K910455 IMS DISPOSABLE HOLDER WITH NEEDLE RETRACTOR
K902196 MODIFIED STICK-GARD SAFETY NEEDLE
K894021 MOBILE X-RAY UNIT
K894041 PUMP-JECT SYRINGE WITH LUER-LOCK
K890620 STICK-GARD SAFETY NEEDLE
K882133 MAMMO M
K843311 IV ADMIN. SET FOR MVP 1 INFUSION PUMP
K842263 MTP E.V. INFUSION PUMP
K831407 CARDIAC OUTPUT COMPUTER
Search all 16 clearances from Ziehm International, Inc. →