Atlas FDA

MicroScan Prompt Inoculation System-D

FDA 510(k) clearance K221493 · decided 2023-04-05

Clearance details

K-number
K221493
Device name
MicroScan Prompt Inoculation System-D
Applicant
Beckman Coulter, Inc.
Decision
Substantially Equivalent
Date received
2022-05-23
Decision date
2023-04-05
Days to decision
317 days
Clearance type
Traditional
Product code
LIE
Device class
2
Regulation number
866.1640
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
THE SENSITITRE AIM (K103456)Trek Diagnostic Systems2011-06-22
SENSITITRE AIM (TM) (K110331)Trek Diagnostic Systems, Ltd.2011-04-27
SENSI-CAL AMCO AEPA-1 (K935566)Radiometer America, Inc.1994-03-29
TURBIDOMETRIC STANDARD (K911059)Scientific Device Laboratory, Inc.1991-06-10
DIFCO DIRECTOR INOCULATION SYSTEM (K890339)Difco Laboratories, Inc.1989-02-07
PROMPT INOCULATION SYSTEM (K820299)3M Company1982-03-15

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Access AFP (on DxI 9000 Analyzer) (P980041/S051)Beckman Coulter, Inc.2025-11-03
Access HBsAg, Access HBsAg Confirmatory, Access HBsAg Calibrator, Access HBsAg QC (P230015)Beckman Coulter, Inc.2025-10-17
Access Hybritech p2PSA (P090026/S032)Beckman Coulter, Inc.2025-06-16
Access Hybritech free PSA (P970038/S046)Beckman Coulter, Inc.2025-05-15
Access Hybritech PSA (P850048/S060)Beckman Coulter, Inc.2024-09-04
Access Hybritech PSA reagent pack (P850048/S059)Beckman Coulter, Inc.2023-05-25
Access AFP Reagents on the Access Immunoassay Systems (P980041/S050)Beckman Coulter, Inc.2022-12-16
Access Hybritech PSA Reagents on the Access Immunoassay Systems (P850048/S057)Beckman Coulter, Inc.2022-12-16