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Advanced Micro-Osmometer Model 3300

by Advanced Instruments, Inc.

510(k) K962056

Advanced Micro-Osmometer Model 3300 is a Class I device made by Advanced Instruments, Inc., cleared under FDA 510(k) K962056 on 11 Jul 1996, active as of 9 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 9 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 9 Oct 2026.

Regulatory status

as of registry sync 9 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK962056 Date11 Jul 1996ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
JJM
Device class
Class I
Regulation
21 CFR Part 862.2730
Advisory committee
Clinical Chemistry
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code JJM (Osmometer For Clinical Use).

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