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STRYKER INTERPULSE HANDPIECE SET, IRRIGATION TIPS, SPLASH SHIELDS, CANAL VISION TIP, IRRIGATION & SUCTION TIPS

K951666 Class II Traditional
Decision Date
1995-09-19
Sponsor / Applicant
Stryker Instruments

Technical Specification

510(k) Submission ID K951666
Product Code FQH
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5475
Decision Date 1995-09-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRYKER INTERPULSE HANDPIECE SET, IRRIGATION TIPS, SPLASH SHIELDS, CANAL VISION TIP, IRRIGATION & SUCTION TIPS received FDA 510(k) clearance under submission number K951666, sponsored by Stryker Instruments. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1995-09-19.

Classification & Regulation

This clearance is catalogued under FDA product code FQH and 21 CFR 880.5475, within the General Hospital review panel as a Class II device.