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FDA 510(k)

CHIROPRATIC INFRA-RED CRYSTAL PAK

K-Number: K821524 · 1982-09-08

ApplicantDr. John D. Reid B.A., D.C.
Decision Date1982-09-08
Product CodeKYA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CHIROPRATIC INFRA-RED CRYSTAL PAK is the device name listed in this FDA 510(k) record. The listed applicant is Dr. John D. Reid B.A., D.C.. It received FDA 510(k) clearance on 1982-09-08 under 510(k) number K821524. The device is classified under product code KYA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHIROPRATIC INFRA-RED CRYSTAL PAK?

CHIROPRATIC INFRA-RED CRYSTAL PAK is a medical device that received FDA 510(k) clearance on 1982-09-08. The listed applicant is Dr. John D. Reid B.A., D.C.. The 510(k) number is K821524.

When did CHIROPRATIC INFRA-RED CRYSTAL PAK receive FDA 510(k) clearance?

CHIROPRATIC INFRA-RED CRYSTAL PAK received FDA 510(k) clearance on 1982-09-08, under 510(k) number K821524.

Who is the listed applicant for CHIROPRATIC INFRA-RED CRYSTAL PAK?

The FDA 510(k) record lists Dr. John D. Reid B.A., D.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHIROPRATIC INFRA-RED CRYSTAL PAK?

The FDA product code for CHIROPRATIC INFRA-RED CRYSTAL PAK is KYA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Dr. John D. Reid B.A., D.C. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K837100DIGITIZING COLORIZING APPLE COMPUTER SYSTEM FOR RE-VIEW OF NORMAL ROENTGEN FILM

Related Devices (Code: KYA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K900404VARICOSCREEN(TM)Promedex, Inc.K832989BREAST THERMAL ACTIVITY INDICATORBcsi Laboratories, Inc.K823245THERMAX; THERMAX SYSTEMAmerican Thermometer Company, Inc.K821049PARATHERMAmerican Thermometer Company, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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