The following data is part of a premarket notification filed by Activator Methods International, Ltd with the FDA for Fs Activator Iii.
| Device ID | K003185 |
| 510k Number | K003185 |
| Device Name: | FS ACTIVATOR III |
| Classification | Manipulator, Plunger-like Joint |
| Applicant | ACTIVATOR METHODS INTERNATIONAL, LTD 3714 EAST INDIAN SCHOOL RD. Phoenix, AZ 85018 |
| Contact | Arlan W Fuhr |
| Correspondent | Arlan W Fuhr ACTIVATOR METHODS INTERNATIONAL, LTD 3714 EAST INDIAN SCHOOL RD. Phoenix, AZ 85018 |
| Product Code | LXM |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-10-11 |
| Decision Date | 2001-03-20 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00850021303136 | K003185 | 000 |
| 00850021303129 | K003185 | 000 |
| 00850021303112 | K003185 | 000 |
| 00850021303105 | K003185 | 000 |
| 00850021303099 | K003185 | 000 |
| 00850021303082 | K003185 | 000 |
| 00850021303051 | K003185 | 000 |
| 00850021303013 | K003185 | 000 |