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510(k) K760052

KIT, PREP SHAVE by M-C Ind., Inc. — Product Code LDQ

K760052 is an FDA 510(k) premarket notification submitted by M-C Ind., Inc. for the device "KIT, PREP SHAVE". The FDA issued a decision of Substantially Equivalent on July 16, 1976. M-C Ind., Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 16, 1976
Date Received
June 15, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by M-C Ind., Inc.

  • K760047 — TRAY, BLADDER IRRIGATION (March 1, 1977)
  • K760048 — TRAY, URETHRAL CATHETERIZATION (March 1, 1977)
  • K760051 — TRAY, SUTURE REMOVAL (August 30, 1976)

Other clearances for product code LDQ

  • K993797 — EC-7701 FLUID WARMING CABINET (January 20, 2000)
  • K992258 — HOT SHOT FLUID WARMER IV FLUIDS (January 12, 2000)
  • K981032 — PIV SYSTEM (September 2, 1998)
  • K973747 — CONTROLLED TEMPERATURE CABINET SYSTEM (May 7, 1998)
  • K955661 — ACU-HALT (December 30, 1996)
  • K955776 — ACU-LAB (June 5, 1996)
  • K945374 — ACU-HALT (August 9, 1995)
  • K944961 — PERSONAL ALARM SYSTEM (PAS) (August 7, 1995)
  • K942810 — PALCO LABS COLD POUCH (June 28, 1995)
  • K930884 — MEDICAL PROCEDURE TRAY, MODIFICATION (March 21, 1995)

FDA data resources