The following data is part of a premarket notification filed by Moldex/metric, Inc. with the FDA for Moldex Health Care N95 Particulate Respirators And Surgical Masks.
Device ID | K062663 |
510k Number | K062663 |
Device Name: | MOLDEX HEALTH CARE N95 PARTICULATE RESPIRATORS AND SURGICAL MASKS |
Classification | Respirator, Surgical |
Applicant | MOLDEX/METRIC, INC. 10111 WEST JEFFERSON BLVD. Culver City, CA 90232 |
Contact | William Wawrzyniak |
Correspondent | Neil E Devine INTERTEK TESTING SERVICES 2307 EAST AURORA ROAD UNIT B7 Twinsburg, OH 44087 |
Product Code | MSH |
CFR Regulation Number | 878.4040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2006-09-07 |
Decision Date | 2006-10-11 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
50092311221767 | K062663 | 000 |
50092311221262 | K062663 | 000 |
50092311221163 | K062663 | 000 |
00092311221007 | K062663 | 000 |