• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

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


New Search Back To Search Results
Device Classification Name Tape And Bandage, Adhesive
510(k) Number K885205
Device Name AQUADERM
Applicant
LAIVAN CORP.
49 FRONT ST.
P.O. BOX 175
EAST ROCKAWAY,  NY  11518
Applicant Contact JOEL MARTZ
Correspondent
LAIVAN CORP.
49 FRONT ST.
P.O. BOX 175
EAST ROCKAWAY,  NY  11518
Correspondent Contact JOEL MARTZ
Regulation Number880.5240
Classification Product Code
KGX  
Date Received12/19/1988
Decision Date 03/29/1989
Decision SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-