Atlas FDA

HEMATASTAT C-70B

FDA 510(k) clearance K913128 · decided 1991-09-23

Clearance details

K-number
K913128
Device name
HEMATASTAT C-70B
Applicant
Separation Technology, Inc.
Decision
Substantially Equivalent
Date received
1991-05-10
Decision date
1991-09-23
Days to decision
136 days
Clearance type
Traditional
Product code
GKG
Device class
2
Regulation number
864.6400
Medical specialty
Hematology
Advisory committee
Hematology
Location
Salt Lake City, UT, 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
SPUNCRIT (K925863)bioMerieux, Inc.1993-02-05
HERMLE Z230H (K920207)Labnet Intl., Inc.1992-06-09
CRITSPIN MICRO-HEMATOCRIT (K920759)Stat-Spin Technologies1992-04-29
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.