The following data is part of a premarket notification filed by Harrison Cbp Seminars with the FDA for Harrison Hand Held Adjusting Instrument.
Device ID | K010851 |
510k Number | K010851 |
Device Name: | HARRISON HAND HELD ADJUSTING INSTRUMENT |
Classification | Manipulator, Plunger-like Joint |
Applicant | HARRISON CBP SEMINARS P.O. BOX 1590 Evanston, WY 82931 -1590 |
Contact | Sang Harrison |
Correspondent | Sang Harrison HARRISON CBP SEMINARS P.O. BOX 1590 Evanston, WY 82931 -1590 |
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 | 2001-03-21 |
Decision Date | 2001-09-18 |