meddevicedb.com FDA Device Reference

PULMONARY FORCED FLOW SYSTEM (PUFFS)

K883008 Class II Traditional
Decision Date
1988-09-29
Sponsor / Applicant
Medical Associated Services, Inc.

Technical Specification

510(k) Submission ID K883008
Product Code BTY
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1890
Decision Date 1988-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PULMONARY FORCED FLOW SYSTEM (PUFFS) received FDA 510(k) clearance under submission number K883008, sponsored by Medical Associated Services, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1988-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code BTY and 21 CFR 868.1890, within the Anesthesiology review panel as a Class II device.