510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900401Substantially Equivalent

Nas&p Grasping Forceps & Assoc. Devices

North American Sterilization & Packaging Co., Sparta NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900401 is the FDA 510(k) clearance record for NAS&P GRASPING FORCEPS & ASSOC. DEVICES, a class I device, cleared for North American Sterilization & Packaging Co. on under FDA product code KOQ (Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)). FDA records list 16 510(k) clearances for North American Sterilization & Packaging Co., from to . As of , FDA records show no recalls naming K900401.

Clearance record

Decision date
Received
(11 days to decision)
Product code
KOQ Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)
Regulation
21 CFR 872.3410
Device class
Class I
Review panel
Dental
Applicant
North American Sterilization & Packaging Co. 15 White Lake Rd., Sparta NJ
Third party review
No

Clearances, product code KOQ

Trailing 12 months

FDA records hold no clearances under product code KOQ in the trailing twelve months.

FDA records show no clearances under product code KOQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KOQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260