KINDERWRAP— 510(k) K872003

Substantially Equivalent

The Kinder Co.

FDA 510(k) clearance K872003 for KINDERWRAP, Substantially Equivalent on 1987-06-23. Applicant: The Kinder Co.. Device class: 1.

Clearance details

Applicant: The Kinder Co.
Product code: Code GAX
Device class: Class 1
Regulation: 21 CFR 878.5900
Advisory panel: General, Plastic Surgery
Date received: 1987-05-26
Decision date: 1987-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ypsilanti, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GAX

K931198 — UNIQUET1993-09-01
K881398 — TOURNIQUET1988-04-29
K881176 — STERILE ESMARCH BANDAGE1988-04-11
K875092 — DEGANIA SILICONE TOURNIQUET1988-01-07
K873928 — UNIVERSAL TOURNIQUET1987-10-23

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