510(k) K944031

VIDEO SCOPE SYSTEM (OTOSCOPE) by Jedmed Instrument Co. — Product Code ERA

K944031 is an FDA 510(k) premarket notification submitted by Jedmed Instrument Co. for the device "VIDEO SCOPE SYSTEM (OTOSCOPE)". The FDA issued a decision of Substantially Equivalent on September 23, 1994. The device falls under product code ERA (Otoscope), a Class I device regulated under 21 CFR 874.4770. Jedmed Instrument Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 23, 1994
Date Received
August 17, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Otoscope
Device Class
Class I
Regulation Number
874.4770
Review Panel
EN
Submission Type