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Osmometer Model 110

by Advanced Instruments, Inc.

510(k) K873642

Osmometer Model 110 is a Class I device made by Advanced Instruments, Inc., cleared under FDA 510(k) K873642 on 20 Oct 1987, active as of 10 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 10 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 10 Oct 2026.

Regulatory status

as of registry sync 10 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK873642 Date20 Oct 1987ClearedStatusActive

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  • Withdrawn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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