TODD MEDICAL/SKILLED CARE PRODUCTS— 510(k) K873469

Name: FDA 510(k) clearance K873469
Creator: U.S. Food and Drug Administration
Published: 1987-10-29

Substantially Equivalent

Todd Medical, Inc.

FDA 510(k) clearance K873469 for TODD MEDICAL/SKILLED CARE PRODUCTS, Substantially Equivalent on 1987-10-29. Applicant: Todd Medical, Inc.. Device class: 1.

Clearance details

Applicant: Todd Medical, Inc.
Product code: Code LRP
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-08-28
Decision date: 1987-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brown Deer, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRP

view all

K963723 — LACERATION TRAY1996-11-27
K951811 — OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK1995-05-31
K940239 — EYE TRAY1994-06-28
K935621 — CUSTOM ENT PACKS1994-03-30
K940646 — ORTHOPEDIC TRAY PRODUCT LINE1994-03-11

More clearances from Todd Medical, Inc.

view all

K873288 — CLOSED FOLEY CATHETER SYSTEM1987-11-27
K873499 — TODD MEDICAL/SKILLED CARE PRODUCTS1987-11-24
K873287 — IRRIGATION TRAY (W/120CC OF STERILE NORMAL SALINE)1987-11-13
K850646 — ECLIPSE SELF ADHERING ELECTRODE1985-09-03
K850004 — TRANSCUTANEOUS NERVE STIMULATOR FOR PAIN RELIEF1985-04-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.