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ASC-952 PHYSIOLOGICAL AMPLIFIER

K894735 Class II Traditional
Decision Date
1989-09-18
Sponsor / Applicant
Astro-Med, Inc.

Technical Specification

510(k) Submission ID K894735
Product Code DRR
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2050
Decision Date 1989-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASC-952 PHYSIOLOGICAL AMPLIFIER received FDA 510(k) clearance under submission number K894735, sponsored by Astro-Med, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-09-18.

Classification & Regulation

This clearance is catalogued under FDA product code DRR and 21 CFR 870.2050, within the Cardiovascular review panel as a Class II device.