Atlas FDA

SPUNCRIT

FDA 510(k) clearance K925863 · decided 1993-02-05

Clearance details

K-number
K925863
Device name
SPUNCRIT
Applicant
bioMerieux, Inc.
Decision
Substantially Equivalent
Date received
1992-11-19
Decision date
1993-02-05
Days to decision
78 days
Clearance type
Traditional
Product code
GKG
Device class
2
Regulation number
864.6400
Medical specialty
Hematology
Advisory committee
Hematology
Location
Bethlehem, PA, 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
SPUNCRIT (MODEL DRC-40) (K961803)Micro Diagnostics Corp.1996-07-05
MULTI-CENTRIFUGE (K955795)Novonx, Inc.1996-03-29
MICROHEMATOCRIT ROTOR (K930415)Fisher Scientific Co., LLC1993-03-23
HERMLE Z230H (K920207)Labnet Intl., Inc.1992-06-09
CRITSPIN MICRO-HEMATOCRIT (K920759)Stat-Spin Technologies1992-04-29
HEMATASTAT C-70B (K913128)Separation Technology, Inc.1991-09-23
HEMATASTAT H-70 (K890849)Separation Technology, Inc.1989-03-21
HCT CENTRIFUGE (K822445)Boehringer Mannheim Corp.1982-09-14
QBC CENTRIFUGAL HEMATOLOGY SYSTEM (K821803)Bd Becton Dickinson Vacutainer Systems Preanalytic1982-09-14
CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY (K813033)Bd Becton Dickinson Vacutainer Systems Preanalytic1982-04-09

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
THXID™-BRAF (P120014/S012)bioMerieux, Inc.2021-12-20
THxID-BRAF kit (P120014/S011)bioMerieux, Inc.2021-03-10
THxID-BRAF assay kit (P120014/S010)bioMerieux, Inc.2020-02-26
THxID BRAF assay kit (P120014/S009)bioMerieux, Inc.2019-08-26
THxID BRAF assay kit (P120014/S008)bioMerieux, Inc.2018-06-27
THxID-BRAF kit (P120014/S007)bioMerieux, Inc.2016-11-22
VIDAS TOTAL PSA (P040008/S013)bioMerieux, Inc.2016-05-31
THXID-BRAF KIT (P120014/S006)bioMerieux, Inc.2016-04-05