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510(k) K900401

NAS&P GRASPING FORCEPS & ASSOC. DEVICES by North American Sterilization & Packaging Co. — Product Code KOQ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 9, 1990
Date Received
January 29, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)
Device Class
Class I
Regulation Number
872.3410
Review Panel
DE
Submission Type

Other clearances by North American Sterilization & Packaging Co.

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  • K963753 — NASP TRANSPARENT DRESSING (November 29, 1996)
  • K962352 — HYDROGEL SKIN DRESSING (August 2, 1996)
  • K925593 — NORTEC STERILE WATER FOR DEVICE IRRIGATION (December 3, 1993)
  • K925588 — NORTEC STER SALINE-O.9% SODIUM CHLOR FOR DEV IRRI (December 3, 1993)
  • K925161 — NORTEC STERILE WATER FOR CATHETER BALLOON INFLATIO (July 21, 1993)
  • K911865 — NORTEC CONNECTING TUBE SET (November 1, 1991)
  • K911784 — NORTEC ROBERTAZZI NASOPHARYNGEAL AIRWAY (September 23, 1991)
  • K910691 — NORTEC URETERAL STENT (August 15, 1991)
  • K903162 — FLEXIBLE ENDOSCOPIC ELECTRODES (December 18, 1990)

Other clearances for product code KOQ

  • K901882 — URESIL ENDOSCOPIC LASER OVERTUBE (July 27, 1990)
  • K896821 — OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE (February 9, 1990)
  • K831265 — DENTOLOCK DENTURE ADHESIVE CREAM (May 9, 1983)