The following data is part of a premarket notification filed by Polamedco, Inc. with the FDA for Polamedco Nasopaharyngeal Airway.
Device ID | K900456 |
510k Number | K900456 |
Device Name: | POLAMEDCO NASOPAHARYNGEAL AIRWAY |
Classification | Airway, Nasopharyngeal |
Applicant | POLAMEDCO, INC. 8295 S.LA CIENEGA BLVD. Inglewood, CA 90301 -1521 |
Contact | Linder, Md |
Correspondent | Linder, Md POLAMEDCO, INC. 8295 S.LA CIENEGA BLVD. Inglewood, CA 90301 -1521 |
Product Code | BTQ |
CFR Regulation Number | 868.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-01-30 |
Decision Date | 1990-04-19 |