Atlas FDA

CARDIOTOMY FILTER

FDA 510(k) clearance K830634 · decided 1983-06-30

Clearance details

K-number
K830634
Device name
CARDIOTOMY FILTER
Applicant
Texas Medical Products, Inc.
Decision
Substantially Equivalent
Date received
1983-03-01
Decision date
1983-06-30
Days to decision
121 days
Clearance type
Traditional
Product code
JOD
Device class
2
Regulation number
870.4270
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
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
GAS FILTER (K993060)Olson Medical Sales, Inc.2000-03-28
CARDIOTOMY/AUTOTRANSFUSION/PLEURAL DRAINAGE VENOUS (K890504)Gish Biomedical, Inc.1989-03-10
PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE (K875095)Pall Biomedical Products Co.1988-02-29
PALL STAT PRIME(TM) BLOOD FILTER FOR EXTRA. USE (K874405)Pall Biomedical Products Co.1987-12-30
SWANK CARDIOTOMY SUCTION LINE BLOOD FILTER CA100 (K855067)Cobe Laboratories, Inc.1986-02-26
CARDIO METRICS CARDIOTOMY RESERVOIR (K841958)Sterile Design, Inc.1984-10-15
INTERFACE CARDIOTOMY BLOOD FILTER #50 (K823259)Medical, Inc.1982-11-24
INTERFACE CARDIOTOMY BLOOD FILTER #51 (K823260)Medical, Inc.1982-11-24
INTERFACE CARDIOTOMY BLOOD FILTER #51 (K812243)Medical, Inc.1981-08-25
INTERFACE CARDIOTOMY BLOOD FILTER (K781383)Medical, Inc.1978-09-27
EXTRACORPEAL CARDIOTOMY BLOOD FILTER (K780653)Cobe Laboratories, Inc.1978-06-14

Recalls involving this device

No recalls on record reference this clearance.