Atlas FDA

OSMOMETER MODEL 110

FDA 510(k) clearance K873642 · decided 1987-10-20

Clearance details

K-number
K873642
Device name
OSMOMETER MODEL 110
Applicant
Advanced Instruments, Inc.
Decision
Substantially Equivalent
Date received
1987-09-09
Decision date
1987-10-20
Days to decision
41 days
Clearance type
Traditional
Product code
JJM
Device class
1
Regulation number
862.2730
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Needham Heights, MA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
THE ADVANCED OSMOMETER (3900) (K965036)Advanced Instruments, Inc.1997-02-20
ADVANCED MICRO-OSMOMETER MODEL 3300 (K962056)Advanced Instruments, Inc.1996-07-11
MODEL 3D3 OSMOMETER (K925970)Advanced Instruments, Inc.1993-07-09
OSMOMETER MODEL 2400 (K911092)Advanced Instruments, Inc.1991-05-22
AO-10 AUTOMATED OSMOMETER (K843997)bioMerieux, Inc.1984-10-31
OSMOTIC PRESSURE AUTO & STAT OM-6010 (K842750)Kyoto Diagnostics, Inc.1984-08-17
WESCOR 5500 VAPOR PRESSURE OSMOMETER (K834214)Wescor, Inc.1984-03-30
COLLOID OSMOMETER 4400 (K834208)Wescor, Inc.1984-03-23
MICRO-SAMPLE OSMOMETER 3M0 (K832783)Advanced Instruments, Inc.1983-11-28
OSMOMETER MODEL OM-6010 (K811179)Fiske Med Science1981-05-15
OSMOMETER MODEL 3W11 (K790611)Advanced Instruments, Inc.1979-06-15

Recalls involving this device

No recalls on record reference this clearance.