The following data is part of a premarket notification filed by Westridge Laboratories, Inc. with the FDA for Id Millennium, Id Moments Silicone.
Device ID | K141767 |
510k Number | K141767 |
Device Name: | ID MILLENNIUM, ID MOMENTS SILICONE |
Classification | Lubricant, Personal |
Applicant | WESTRIDGE LABORATORIES, INC. 27001 LA PAZ ROAD, SUITE 312 Mission Viejo, CA 92691 |
Contact | Albert Rego |
Correspondent | Albert Rego WESTRIDGE LABORATORIES, INC. 27001 LA PAZ ROAD, SUITE 312 Mission Viejo, CA 92691 |
Product Code | NUC |
CFR Regulation Number | 884.5300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-07-01 |
Decision Date | 2015-03-09 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00761236900891 | K141767 | 000 |
30864785000225 | K141767 | 000 |
30864785000232 | K141767 | 000 |
00761236109867 | K141767 | 000 |
00761236109898 | K141767 | 000 |
00761236109928 | K141767 | 000 |
40761236900059 | K141767 | 000 |
40761236900608 | K141767 | 000 |
40761236900615 | K141767 | 000 |
30761236900625 | K141767 | 000 |
30761236900632 | K141767 | 000 |
20761236900741 | K141767 | 000 |
10761236900829 | K141767 | 000 |
00840281300099 | K141767 | 000 |