Delta Rolling Self-Licking Walker

FDA 510(k) K792064 · Staricat, Inc.

Substantially Equivalent

510(k) numberK792064

Submission

Device name
Delta Rolling Self-Licking Walker
Applicant
Staricat, Inc.
Mchenry, IL, US
Received
October 15, 1979
Decision date
October 30, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
ITJ – Walker, Mechanical
Device class
Class I (low risk)
Regulation
21 CFR 890.3825
Specialty
Physical Medicine

Other 510(k)s with product code ITJ

510(k)DeviceApplicantDecision
K833869Child's WalkerITJ · Traditional Kaye Products, Inc.11/29/1983SE
K833195Umbrella WalkerITJ · Traditional Convaid Products, Inc.10/27/1983SE
K830784Walk N RollITJ · Traditional Meta-Morris05/25/1983SE
K830848Resi-WalkerITJ · Traditional Lic-Orthion04/05/1983SE
K823105Resi-WalkerITJ · Traditional Orthion Corp.11/05/1982SE
K821404Light Weight Aluminum WalkerITJ · Traditional Manuco Manufacturing Co., Inc.05/21/1982SE
K820711Walk-A-CycleITJ · Traditional Walk-A-Cycle Division04/08/1982SE
K811485Walker/Crutch BagITJ · Traditional Fred Sammons, Inc.06/16/1981SE
K790529Walking AidITJ · Traditional Maddak, Inc.04/03/1979SE
K772049Walking AidITJ · Traditional Guardian Products Co., Inc.11/11/1977SE

Questions and answers

When was Delta Rolling Self-Licking Walker cleared by the FDA?

Delta Rolling Self-Licking Walker (K792064) received a 510(k) decision of Substantially Equivalent on October 30, 1979, 15 days after the submission was received.

What is the product code of K792064?

The FDA product code is ITJ – Walker, Mechanical, a Class I (low risk) device regulated under 21 CFR 890.3825.