Atlas FDA

LABOTECH AUTOMATED MICROTITER ANALYZER

FDA 510(k) clearance K922081 · decided 1992-09-02

Clearance details

K-number
K922081
Device name
LABOTECH AUTOMATED MICROTITER ANALYZER
Applicant
Innovative Medical Systems, Inc.
Decision
Substantially Equivalent
Date received
1992-05-05
Decision date
1992-09-02
Days to decision
120 days
Clearance type
Traditional
Product code
JJQ
Device class
1
Regulation number
862.2300
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Warren, NJ, 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
UBIT-IR300 INFRARED SPECTROMETRY SYSTEM (K013371)Otsuka Pharmaceutical Co., Ltd.2001-12-21
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ANTHOS PHACTS VERSION MICROPLATE READER (K962113)Columbia Bioscience, Inc.1996-11-05
CBI 7520 READER (K961183)Columbia Bioscience, Inc.1996-08-02
ORIGEN ANALYZER (K962166)Igen, Inc.1996-07-31
ANTHOS 2010 READER (K955077)Anthos Labtec, Inc.1995-12-04
ELX808 AUTOMATED MICROPLATE READERS (K953710)Bio-Tek Instruments, Inc.1995-10-25
ELX800UV (K953572)Bio-Tek Instruments, Inc.1995-10-19
BILI-METER (K953005)Olympic Medical Corp.1995-09-28
5STRATEC SL 300 LIA-MAT (K950029)Nichols Institute Diagnostics1995-08-02

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
SHARPX NEEDLE DESTRUCTION UNIT (P980015/S005)Innovative Medical Systems, Inc.2002-06-12
SHARPX NEEDLE DESTRUCTION UNIT (P980015/S004)Innovative Medical Systems, Inc.2001-08-15
SHARP(X)TM NEEDLE DESTRUCTION UNIT (P980015/S003)Innovative Medical Systems, Inc.1999-09-17
SHARP NEEDLE DESTRUCTION UNIT (P980015/S002)Innovative Medical Systems, Inc.1999-03-19
SHARP NEEDLE DESTRUCTION UNIT (P980015/S001)Innovative Medical Systems, Inc.1998-12-14
SHARPX (P980015)Innovative Medical Systems, Inc.1998-08-06