The following data is part of a premarket notification filed by Fisher & Paykel Healthcare, Ltd. with the FDA for Infosend Gsm.
Device ID | K110316 |
510k Number | K110316 |
Device Name: | INFOSEND GSM |
Classification | Ventilator, Non-continuous (respirator) |
Applicant | FISHER & PAYKEL HEALTHCARE, LTD. 15 MAURICE PAYKEL PLACE, EAST TAMAKI Auckland, NZ 1701 |
Contact | James Thompson |
Correspondent | James Thompson FISHER & PAYKEL HEALTHCARE, LTD. 15 MAURICE PAYKEL PLACE, EAST TAMAKI Auckland, NZ 1701 |
Product Code | BZD |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-02-03 |
Decision Date | 2011-08-19 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
09420012448019 | K110316 | 000 |
09420012425218 | K110316 | 000 |