Atlas FDA

FINGER TOURNIQUETTE

FDA 510(k) clearance K853472 · decided 1985-10-10

Clearance details

K-number
K853472
Device name
FINGER TOURNIQUETTE
Applicant
Joseph B. Marogil
Decision
Substantially Equivalent
Date received
1985-08-20
Decision date
1985-10-10
Days to decision
51 days
Clearance type
Traditional
Product code
GAX
Device class
1
Regulation number
878.5900
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Grand Rapids, MI, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
UNIQUET (K931198)Icat Systems1993-09-01
TOURNIQUET (K881398)Barretta Products, Research and Development, Inc.1988-04-29
STERILE ESMARCH BANDAGE (K881176)Spectrum/Hydro-Med Products, Inc.1988-04-11
DEGANIA SILICONE TOURNIQUET (K875092)Degania Silicone , Ltd.1988-01-07
UNIVERSAL TOURNIQUET (K873928)Dryden Corp.1987-10-23
KINDERWRAP (K872003)The Kinder Co.1987-06-23
DALE VENIPUNCTURE TOURNIQUET, PRODUCT NO. 1335 (K864897)Dale Medical Products, Inc.1987-01-12
VELCRO TOURNIQUET (K853537)Cp Medical1985-09-12
CATAPRESS TOURNIGUET (K852277)Boehringer Ingelheim Pharmaceuticals, Inc.1985-06-27
TOURNIQUET (K851482)Polymer Technology Corp.1985-04-29
ELASTIC BANDAGE (K843056)Sterile Medical Systems1984-12-04
DISPOSIQUET A DISPOS. TOURNIQUET (K840489)Med Lab Products1984-03-12

Recalls involving this device

RecordFirmDate
Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - P recall (Z-0945-2021)Mar-Med Co2021-02-02