The following data is part of a premarket notification filed by Micromed Development Corp. with the FDA for Collar Button Venturi Vent Tube.
Device ID | K943848 |
510k Number | K943848 |
Device Name: | COLLAR BUTTON VENTURI VENT TUBE |
Classification | Tube, Tympanostomy |
Applicant | MICROMED DEVELOPMENT CORP. 4911 CREEKSIDE DR. Clearwater, FL 34620 |
Contact | Dan H Treace |
Correspondent | Dan H Treace MICROMED DEVELOPMENT CORP. 4911 CREEKSIDE DR. Clearwater, FL 34620 |
Product Code | ETD |
CFR Regulation Number | 874.3880 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-08-04 |
Decision Date | 1994-09-16 |