510(k) K901985

BLOOD GAS CONTROLS by Phoenix Diagnostics, Inc. — Product Code JJS

K901985 is an FDA 510(k) premarket notification submitted by Phoenix Diagnostics, Inc. for the device "BLOOD GAS CONTROLS". The FDA issued a decision of Substantially Equivalent on June 6, 1990. The device falls under product code JJS (Controls For Blood-Gases, (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Phoenix Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 6, 1990
Date Received
May 2, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Controls For Blood-Gases, (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type