510(k) K932006

1500 SERIES REGULATOR by Precision Medical, Inc. — Product Code CAN

K932006 is an FDA 510(k) premarket notification submitted by Precision Medical, Inc. for the device "1500 SERIES REGULATOR". The FDA issued a decision of Substantially Equivalent on October 25, 1993. The device falls under product code CAN (Regulator, Pressure, Gas Cylinder), a Class I device regulated under 21 CFR 868.2700. Precision Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 1993
Date Received
April 21, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Regulator, Pressure, Gas Cylinder
Device Class
Class I
Regulation Number
868.2700
Review Panel
AN
Submission Type