Skip to content

Osmometer Model 2400

by Advanced Instruments, Inc.

510(k) K911092

Osmometer Model 2400 is a Class I device made by Advanced Instruments, Inc., cleared under FDA 510(k) K911092 on 22 May 1991, 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 NumberK911092 Date22 May 1991ClearedStatusActive

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  • Withdrawn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).

Other devices from Advanced Instruments, LLC

See all devices from Advanced Instruments, LLC →