Atlas FDA

ARTERIAL BLOOD SAMPLING KIT

FDA 510(k) clearance K821406 · decided 1982-06-25

Clearance details

K-number
K821406
Device name
ARTERIAL BLOOD SAMPLING KIT
Applicant
Dhd Medical Products Div. Diemolding Corp.
Decision
Substantially Equivalent
Date received
1982-05-11
Decision date
1982-06-25
Days to decision
45 days
Clearance type
Traditional
Product code
CBT
Device class
1
Regulation number
868.1100
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
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
HEMODRAW ARTERIAL BLOOD SAMPLING SYSTEM (K071269)Smiths Medical Asd, Inc.2007-08-01
SECURE ARTERIAL BLOOD SAMPLING SYSTEM (K070340)Smiths Medical Asd, Inc.2007-03-15
ABC IN-LINE BLOOD SAMPLING KIT (K955663)Utah Medical Products, Inc.1997-03-17
ABG POINT LOK NEEDLE PROTECTION DEVICE (K954015)Devon Industries, Inc.1995-11-20
ACTI-FLEX ARTERIAL EXTENSION SET (K954035)R-Group Intl.1995-09-25
NEEDLE SAFETY COVER (K950098)Hammer-Plane, Inc.1995-08-11
ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM (K945719)Sherwood Medical Co.1995-03-16
PISTON SYRINGE (K944941)Martell Medical Products, Inc.1994-12-05
ABG NEEDLE PROTECTION (K945485)Devon Industries, Inc.1994-11-29
ASPIR-PULSE(TM) SAF-T-VENT (K940575)Sherwood Medical Co.1994-03-22
VACVENT (K931873)Steven Frank Mercereau1993-12-30
BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560 (K930986)Customed, Inc.1993-07-14

Recalls involving this device

No recalls on record reference this clearance.