The following data is part of a premarket notification filed by Dryden Corp. with the FDA for Breathing Circuit W/heated Wire.
Device ID | K880769 |
510k Number | K880769 |
Device Name: | BREATHING CIRCUIT W/HEATED WIRE |
Classification | Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer |
Applicant | DRYDEN CORP. 10640 EAST 59TH ST. P.O. BOX 36038 Indianapolis, IN 46236 |
Contact | Paul E Dryden |
Correspondent | Paul E Dryden DRYDEN CORP. 10640 EAST 59TH ST. P.O. BOX 36038 Indianapolis, IN 46236 |
Product Code | BZE |
CFR Regulation Number | 868.5270 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-02-29 |
Decision Date | 1988-08-24 |