510(k) K800655

MODEL 100 SPECTRAVIEW by Edwards Laboratories — Product Code DQC

K800655 is an FDA 510(k) premarket notification submitted by Edwards Laboratories for the device "MODEL 100 SPECTRAVIEW". The FDA issued a decision of Substantially Equivalent on April 16, 1980. The device falls under product code DQC (Phonocardiograph), a Class I device regulated under 21 CFR 870.2390. Edwards Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 16, 1980
Date Received
March 25, 1980
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