The following data is part of a premarket notification filed by Interlace Medical, Inc. with the FDA for Myosure Rod Lens Scope Seals.
Device ID | K102686 |
510k Number | K102686 |
Device Name: | MYOSURE ROD LENS SCOPE SEALS |
Classification | Hysteroscope (and Accessories) |
Applicant | INTERLACE MEDICAL, INC. 139 NEWBURY STREET Framingham, MA 01701 |
Contact | John J Vozella |
Correspondent | John J Vozella INTERLACE MEDICAL, INC. 139 NEWBURY STREET Framingham, MA 01701 |
Product Code | HIH |
CFR Regulation Number | 884.1690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-09-17 |
Decision Date | 2010-10-15 |
Summary: | summary |