Atlas FDA

GRAM NEGATIVE FLUORESCENT IDENTIFICATION PANEL

FDA 510(k) clearance K862642 · decided 1986-09-11

Clearance details

K-number
K862642
Device name
GRAM NEGATIVE FLUORESCENT IDENTIFICATION PANEL
Applicant
American Micro Scan
Decision
Substantially Equivalent
Date received
1986-07-11
Decision date
1986-09-11
Days to decision
62 days
Clearance type
Traditional
Product code
LQM
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
West Sacramento, CA, 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
ROCHE OXI/FERM II (K923313)Roche Diagnostic Systems, Inc.1993-04-05
VITEK RAPID CALL-GRAM NEGATIV IDENT CARD (K925915)Biomerieux Vitek, Inc.1993-03-23
SCEPTOR IDENTIFICATION SYSTEM (K912897)Bd Becton Dickinson Vacutainer Systems Preanalytic1991-10-28
VITEK GRAM NEGATIVE IDENTIFICATION CARD, MODIFIED (K911429)Vitek Systems, Inc.1991-06-24
SENSITITRE AUTO ID PLATE AP80 (K890057)Radiometer America, Inc.1989-06-09
PASCO GRAM NEGATIVE IDENTIFICATION SYSTEM (K851528)Pasco Laboratories, Inc.1985-07-15

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
MIC PANELS (N62160/S013)American Micro Scan1985-03-05
MIC PANELS (N62160/S011)American Micro Scan1984-01-30
MIC PANELS (N62160/S012)American Micro Scan1984-01-30
MIC PANELS (N62160/S010)American Micro Scan1983-10-12
MIC PANELS (N62160/S009)American Micro Scan1983-09-28
MIC PANELS (N62160/S008)American Micro Scan1983-08-10
MIC PANELS (N62160/S007)American Micro Scan1983-02-03
MIC PANELS (N62160/S006)American Micro Scan1982-11-18