The following data is part of a premarket notification filed by Dr. John D. Reid B.a., D.c. with the FDA for Chiropratic Infra-red Crystal Pak.
Device ID | K821524 |
510k Number | K821524 |
Device Name: | CHIROPRATIC INFRA-RED CRYSTAL PAK |
Classification | System, Thermographic, Liquid Crystal, Nonpowered (adjunctive Use) |
Applicant | DR. JOHN D. REID B.A., D.C. 803 N. Front St. Suite 3 McHenry, IL 60050 |
Product Code | KYA |
CFR Regulation Number | 884.2982 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-05-21 |
Decision Date | 1982-09-08 |