The following data is part of a premarket notification filed by Boston Medical Products, Inc. with the FDA for Custom Nasal Splint.
Device ID | K972082 |
510k Number | K972082 |
Device Name: | CUSTOM NASAL SPLINT |
Classification | Splint, Intranasal Septal |
Applicant | BOSTON MEDICAL PRODUCTS, INC. 117 FLANDERS RD. Westborough, MA 01581 |
Contact | Stuart K Montgomery |
Correspondent | Stuart K Montgomery BOSTON MEDICAL PRODUCTS, INC. 117 FLANDERS RD. Westborough, MA 01581 |
Product Code | LYA |
CFR Regulation Number | 874.4780 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-06-04 |
Decision Date | 1997-07-03 |
Summary: | summary |