The following data is part of a premarket notification filed by Eastmed Enterprises Inc. with the FDA for Macintosh Laryngoscope Blades (american Profile).
Device ID | K901489 |
510k Number | K901489 |
Device Name: | MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE) |
Classification | Laryngoscope, Rigid |
Applicant | EASTMED ENTERPRISES INC. 5 PEMBURY COURT Marlton, NJ 08053 |
Contact | Rathin Putatunda |
Correspondent | Rathin Putatunda EASTMED ENTERPRISES INC. 5 PEMBURY COURT Marlton, NJ 08053 |
Product Code | CCW |
CFR Regulation Number | 868.5540 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-03-29 |
Decision Date | 1990-04-10 |