Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K022480
Device Classification Name
Hysteroscope (And Accessories)
More FDA Info for this Device
510(K) Number
K022480
Device Name
Hysteroscope (And Accessories)
Applicant
ACMI CORPORATION
136 TURNPIKE RD.
SOUTHBOROUGH, MA 01772 US
Other 510(k) Applications for this Company
Contact
JOHN A DELUCIA
Other 510(k) Applications for this Contact
Regulation Number
884.1690
More FDA Info for this Regulation Number
Classification Product Code
HIH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/26/2002
Decision Date
08/22/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact