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510(k) K853507

STERI-GRIP by Clinical Technology Corp.

K853507 is an FDA 510(k) premarket notification submitted by Clinical Technology Corp. for the device "STERI-GRIP". The FDA issued a decision of Substantially Equivalent on September 5, 1985. Clinical Technology Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 5, 1985
Date Received
August 21, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Clinical Technology Corp.

  • K925080 — TEK-LUBE (January 31, 1994)
  • K872867 — BIOSIGN (July 6, 1988)
  • K880166 — BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 (February 18, 1988)
  • K872705 — BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) (September 1, 1987)
  • K855138 — BOVIE ULTRASONIC SURGICAL SYSTEM (November 10, 1986)
  • K854231 — ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES (May 2, 1986)
  • K852986 — GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN (August 19, 1985)
  • K844565 — BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT) (February 21, 1985)
  • K841272 — SICKLE-STAT HEMOGLOBIN S SCREEN KIT (April 13, 1984)
  • K823077 — URINARY BLADDER TEMP. SENSOR #81-003 (March 9, 1983)

FDA data resources