The following data is part of a premarket notification filed by D.d. Surgical, Inc. with the FDA for Lasevac.
Device ID | K951490 |
510k Number | K951490 |
Device Name: | LASEVAC |
Classification | Laparoscope, Gynecologic (and Accessories) |
Applicant | D.D. SURGICAL, INC. 404 MARVEL COURT Easton, MD 21601 |
Contact | L. T Divilio |
Correspondent | L. T Divilio D.D. SURGICAL, INC. 404 MARVEL COURT Easton, MD 21601 |
Product Code | HET |
CFR Regulation Number | 884.1720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-03-31 |
Decision Date | 1995-06-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() LASEVAC 74607019 1989289 Dead/Cancelled |
DD Surgical, Inc. 1994-12-05 |