The following data is part of a premarket notification filed by Natus Medical, Inc. with the FDA for Minimuffs.
Device ID | K935160 |
510k Number | K935160 |
Device Name: | MINIMUFFS |
Classification | Protector, Hearing (circumaural) |
Applicant | NATUS MEDICAL, INC. 1501 INDUSTRIAL RD. San Carlos, CA 94070 |
Contact | Lisa Taylor |
Correspondent | Lisa Taylor NATUS MEDICAL, INC. 1501 INDUSTRIAL RD. San Carlos, CA 94070 |
Product Code | EWE |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-10-29 |
Decision Date | 1995-02-09 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MINIMUFFS 77256444 3466145 Live/Registered |
Natus Medical Incorporated 2007-08-15 |
MINIMUFFS 75352102 2208641 Dead/Cancelled |
Natus Medical, Inc. 1997-09-05 |