Atlas FDA

SIMPLATE PEDIATRIC

FDA 510(k) clearance K911745 · decided 1991-08-09

Clearance details

K-number
K911745
Device name
SIMPLATE PEDIATRIC
Applicant
Organon Teknika Corp.
Decision
Substantially Equivalent
Date received
1991-04-18
Decision date
1991-08-09
Days to decision
113 days
Clearance type
Traditional
Product code
JCA
Device class
2
Regulation number
864.6100
Medical specialty
Hematology
Advisory committee
Hematology
Location
Durham, NC, 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
SURGICUTT-BLEEDING TIME DEVICE, MODIFICATION (K911996)International Technidyne Corp.1991-07-17
Q.I.C. BLEEDING TIME DEVICE (K871318)Helena Laboratories1987-06-10
SURGICUTT - BLEEDING TIME DEVICE (K850542)International Technidyne Corp.1985-03-01
BLEEDING TIME DEVICE DISPOSABLE (K830645)American Dade1983-03-17
AUTOLET (K801815)Ulster Scientific, Inc.1980-10-10
SIMPLATE (K761250)General Diagnostics1977-03-01

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
HEPANOSTIKA(TM) ANTI-HAV MIDROELISA SYSTEM (P830018/S001)Organon Teknika Corp.1990-03-21
HEPANOSTIKA(TM) HBEAG/ANTI HBE MICROELISA(TM) SYST (P840070/S001)Organon Teknika Corp.1990-03-21
9EPANOSTIKA(TM) ANTI-HAV IGM (P830017/S001)Organon Teknika Corp.1990-03-21
AUTOBAC MIC TEST SYSTEM (N50524/S033)Organon Teknika Corp.1990-01-22
AUTOBAC MIC TEST SYSTEM (N50524/S035)Organon Teknika Corp.1989-12-07
AUTOBAC MIC TEST SYSTEM (N50524/S032)Organon Teknika Corp.1989-06-13
HEPANOSTIKA(TM) ANTI-HAV MIDROELISA SYSTEM (P830018)Organon Teknika Corp.1989-02-06
AUTOBAC MIC TEST SYSTEM (N50524/S031)Organon Teknika Corp.1988-12-28