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AKTINA MEDICAL PHYSICS CORPORATION TENNIS RACQUET INSERT

K993522 Class II Traditional
Decision Date
2000-01-10
Sponsor / Applicant
Aktina Medical Physics Corp.

Technical Specification

510(k) Submission ID K993522
Product Code JAI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5770
Decision Date 2000-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AKTINA MEDICAL PHYSICS CORPORATION TENNIS RACQUET INSERT received FDA 510(k) clearance under submission number K993522, sponsored by Aktina Medical Physics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-01-10.

Classification & Regulation

This clearance is catalogued under FDA product code JAI and 21 CFR 892.5770, within the Radiology review panel as a Class II device.