The following data is part of a premarket notification filed by Health Care Mfg., Inc. with the FDA for Hcmi X-ray High Requency Chiropractic Radiographic.
Device ID | K022737 |
510k Number | K022737 |
Device Name: | HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC |
Classification | System, X-ray, Stationary |
Applicant | HEALTH CARE MFG., INC. P.O. BOX 7007 Deerfield, IL 60015 |
Contact | Daniel Kamm |
Correspondent | Daniel Kamm HEALTH CARE MFG., INC. P.O. BOX 7007 Deerfield, IL 60015 |
Product Code | KPR |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-08-19 |
Decision Date | 2002-10-22 |
Summary: | summary |