Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Section Content Menu Skip to Common Links
-

510(k) Premarket Notification

Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA
 


New Search Back To Search Results
Device Classification Name laparoscope, general & plastic surgery
510(k) NumberK982445
Device NameMODULAP
Applicant
ATC MEDICAL TECHNOLOGY, INC.
1034 lincoln st.
hollywood,  FL  33019
Contactmarian harding cochran
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received07/15/1998
Decision Date 09/08/1998
Decision substantially equivalent (SE)
Classification Advisory Committee General & Plastic Surgery
Review Advisory Committee General & Plastic Surgery
Statement/Summary/Purged Status Summary only
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
 
-
-
-
-
-