Home / 510(k) Clearances / K873469

510(k) K873469

TODD MEDICAL/SKILLED CARE PRODUCTS by Todd Medical, Inc. — Product Code LRP

K873469 is an FDA 510(k) premarket notification submitted by Todd Medical, Inc. for the device "TODD MEDICAL/SKILLED CARE PRODUCTS". The FDA issued a decision of Substantially Equivalent on October 29, 1987. The device falls under product code LRP (Tray, Surgical), a Class I device regulated under 21 CFR 878.4800. Todd Medical, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 29, 1987
Date Received
August 28, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tray, Surgical
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

Other clearances by Todd Medical, Inc.

  • K873288 — CLOSED FOLEY CATHETER SYSTEM (November 27, 1987)
  • K873499 — TODD MEDICAL/SKILLED CARE PRODUCTS (November 24, 1987)
  • K873287 — IRRIGATION TRAY (W/120CC OF STERILE NORMAL SALINE) (November 13, 1987)
  • K850646 — ECLIPSE SELF ADHERING ELECTRODE (September 3, 1985)
  • K850004 — TRANSCUTANEOUS NERVE STIMULATOR FOR PAIN RELIEF (April 2, 1985)

Other clearances for product code LRP

  • K963723 — LACERATION TRAY (November 27, 1996)
  • K951811 — OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK (May 31, 1995)
  • K940239 — EYE TRAY (June 28, 1994)
  • K935621 — CUSTOM ENT PACKS (March 30, 1994)
  • K940646 — ORTHOPEDIC TRAY PRODUCT LINE (March 11, 1994)
  • K940444 — GENERAL SURGERY TRAY (March 7, 1994)
  • K922126 — HOSPITAL KIT ENT 1125 (January 21, 1993)
  • K912105 — EYE TRAY (August 29, 1991)
  • K903963 — KITS AND TRAYS FOR ONE TIME USE ONLY (July 29, 1991)
  • K903962 — INSTRUMENTS FOR ONE TIME USE/ DISPOSABLE (July 29, 1991)

FDA data resources