510(k) K900365

PAG MICROPROCESSOR-CONTROLLED MODULE by Life Sciences Manufacturing, Inc. — Product Code DQC

K900365 is an FDA 510(k) premarket notification submitted by Life Sciences Manufacturing, Inc. for the device "PAG MICROPROCESSOR-CONTROLLED MODULE". The FDA issued a decision of Substantially Equivalent on July 18, 1990. The device falls under product code DQC (Phonocardiograph), a Class I device regulated under 21 CFR 870.2390. Life Sciences Manufacturing, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 18, 1990
Date Received
January 25, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Phonocardiograph
Device Class
Class I
Regulation Number
870.2390
Review Panel
CV
Submission Type