510(k) K811626

MEDDARS/ULTRA IMAGER PULSE/PHON MODULE by Honeywell, Inc. — Product Code DQC

K811626 is an FDA 510(k) premarket notification submitted by Honeywell, Inc. for the device "MEDDARS/ULTRA IMAGER PULSE/PHON MODULE". The FDA issued a decision of Substantially Equivalent on July 1, 1981. The device falls under product code DQC (Phonocardiograph), a Class I device regulated under 21 CFR 870.2390. Honeywell, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 1, 1981
Date Received
June 9, 1981
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