Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K001275
Device Classification Name
Camera, Ophthalmic, Ac-Powered
More FDA Info for this Device
510(K) Number
K001275
Device Name
Camera, Ophthalmic, Ac-Powered
Applicant
MASSIE RESEARCH LABORATORIES, INC.
6761 SIERRA CT., SUITE E
DUBLIN, CA 94568 US
Other 510(k) Applications for this Company
Contact
BERT MASSIE
Other 510(k) Applications for this Contact
Regulation Number
886.1120
More FDA Info for this Regulation Number
Classification Product Code
HKI
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/20/2000
Decision Date
07/13/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OP - Ophthalmic
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact