Atlas FDA

S/P CAPILLARY TUBES, HEPARINIZED (2A)

FDA 510(k) clearance K812969 · decided 1981-11-06

Clearance details

K-number
K812969
Device name
S/P CAPILLARY TUBES, HEPARINIZED (2A)
Applicant
American Dade
Decision
Substantially Equivalent
Date received
1981-10-22
Decision date
1981-11-06
Days to decision
15 days
Clearance type
Traditional
Product code
GIO
Device class
1
Regulation number
864.6150
Medical specialty
Hematology
Advisory committee
Hematology
Location
Mchenry, IL, 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
QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM (K972969)Innovative Medical Technologies, Inc.1997-09-22
MONOJECT SAMPLETTE SEPARATOR TUBE (K941291)Sherwood Medical Co.1994-10-27
TRU-TRAX (K894851)Humagen, Inc.1989-09-29
HEMA(PRO)TEC(TION) (K885324)Medical Products Search, Inc.1989-02-17
CAPILLARY TUBE, BLOOD COLLECTION (K885138)Coeur Laboratories, Inc.1989-02-07
SAFE-TEC CAPILLARY BLOOD COLLECTION TUBE (K884623)Safe-Tec Clinical Products, Inc.1988-12-01
NATELSON TUBES, HEPARIN AND PLAIN (K881187)Helps Products, Inc.1988-05-06
CARAWAY TUBES, HEPARIN AND PLAIN (K881262)Helps Products, Inc.1988-05-06
MONOJECT SAMPLETTE AMBER CAPILLARY SERUM SEPARATOR (K875061)Sherwood Medical Co.1988-01-12
VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE (K873647)Ventrex Laboratories, Inc.1987-10-20
CORNING BLOOD COLLECTION CAPILLARY TUBES (K850806)Corning Medical & Scientific1985-03-25
CAPILLARY BLOOD COLLECTION TUBE (K843608)Medical Technomics, Ltd.1984-11-30

Recalls involving this device

No recalls on record reference this clearance.