FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TODD MEDICAL/SKILLED CARE PRODUCTS

K Number: K873469 · Decision Oct 29, 1987
Classifications
1
FEI Numbers
285
Registration Numbers
286
Same Product Code
21
Applicant Total
6
Review Days
62

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
TODD MEDICAL/SKILLED CARE PRODUCTS
K Number
K873469
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Todd Medical, Inc.
Date Received
August 28, 1987
Decision Date
October 29, 1987
Product Code
LRP
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
LRP Tray, Surgical

Similar 510(k) Clearances

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

View all

Other Clearances by Todd Medical, Inc.

K Number Device Name
K873288 CLOSED FOLEY CATHETER SYSTEM
K873499 TODD MEDICAL/SKILLED CARE PRODUCTS
K873287 IRRIGATION TRAY (W/120CC OF STERILE NORMAL SALINE)
K850646 ECLIPSE SELF ADHERING ELECTRODE
K850004 TRANSCUTANEOUS NERVE STIMULATOR FOR PAIN RELIEF