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ADVANCED MICRO-OSMOMETER MODEL 3300

K962056 Class I Traditional
Decision Date
1996-07-11
Sponsor / Applicant
Advanced Instruments, Inc.

Technical Specification

510(k) Submission ID K962056
Product Code JJM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2730
Decision Date 1996-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANCED MICRO-OSMOMETER MODEL 3300 received FDA 510(k) clearance under submission number K962056, sponsored by Advanced Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1996-07-11.

Classification & Regulation

This clearance is catalogued under FDA product code JJM and 21 CFR 862.2730, within the Clinical Chemistry review panel as a Class I device.