TOURNEQUET, NON-PNEUMATIC— 510(k) K780429

Substantially Equivalent

Hemox, Inc.

FDA 510(k) clearance K780429 for TOURNEQUET, NON-PNEUMATIC, Substantially Equivalent on 1978-04-18. Applicant: Hemox, Inc.. Device class: 1.

Clearance details

Applicant: Hemox, Inc.
Product code: Code GAX
Device class: Class 1
Regulation: 21 CFR 878.5900
Advisory panel: General, Plastic Surgery
Date received: 1978-03-17
Decision date: 1978-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.