510(k) K945719

ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM by Sherwood Medical Co. — Product Code CBT

K945719 is an FDA 510(k) premarket notification submitted by Sherwood Medical Co. for the device "ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM". The FDA issued a decision of Substantially Equivalent (kit) on March 16, 1995. The device falls under product code CBT (Arterial Blood Sampling Kit), a Class I device regulated under 21 CFR 868.1100. Sherwood Medical Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESK (Substantially Equivalent (kit))
Decision Date
March 16, 1995
Date Received
November 21, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Arterial Blood Sampling Kit
Device Class
Class I
Regulation Number
868.1100
Review Panel
AN
Submission Type

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.