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510(k) K873928

UNIVERSAL TOURNIQUET by Dryden Corp. — Product Code GAX

K873928 is an FDA 510(k) premarket notification submitted by Dryden Corp. for the device "UNIVERSAL TOURNIQUET". The FDA issued a decision of Substantially Equivalent on October 23, 1987. The device falls under product code GAX (Tourniquet, Nonpneumatic), a Class I device regulated under 21 CFR 878.5900. Dryden Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 23, 1987
Date Received
September 25, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tourniquet, Nonpneumatic
Device Class
Class I
Regulation Number
878.5900
Review Panel
SU
Submission Type

Other clearances by Dryden Corp.

  • K880923 — PATIENT VENTILATOR ISOLATOR (September 6, 1988)
  • K880769 — BREATHING CIRCUIT W/HEATED WIRE (August 24, 1988)
  • K882285 — NONREBREATHING CIRCUIT (August 16, 1988)
  • K873927 — REUSEABLE BREATHING TUBES (October 20, 1987)
  • K870859 — BAG-TAIL BLEED VALVE (August 3, 1987)
  • K871386 — BREATHING CIRCUIT (May 29, 1987)
  • K870858 — BADGWELL SAMPLING CATHETER (May 14, 1987)
  • K861540 — DISPOSABLE BERMAN AND GUEDEL AIRWAYS (May 2, 1986)
  • K850644 — NASOPHARYNGEAL AIRWAY-ROBERTAZZI (March 21, 1985)
  • K842843 — DRYDEN SCAVENGER INTERFACE SYSTEM (July 27, 1984)

Other clearances for product code GAX

  • K931198 — UNIQUET (September 1, 1993)
  • K881398 — TOURNIQUET (April 29, 1988)
  • K881176 — STERILE ESMARCH BANDAGE (April 11, 1988)
  • K875092 — DEGANIA SILICONE TOURNIQUET (January 7, 1988)
  • K872003 — KINDERWRAP (June 23, 1987)
  • K864897 — DALE VENIPUNCTURE TOURNIQUET, PRODUCT NO. 1335 (January 12, 1987)
  • K853472 — FINGER TOURNIQUETTE (October 10, 1985)
  • K853537 — VELCRO TOURNIQUET (September 12, 1985)
  • K852277 — CATAPRESS TOURNIGUET (June 27, 1985)
  • K851482 — TOURNIQUET (April 29, 1985)

FDA data resources