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FDA 510(k)

HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC

K-Number: K022737 · 2002-10-22

ApplicantHealth Care Mfg., Inc.
Decision Date2002-10-22
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC is the device name listed in this FDA 510(k) record. The listed applicant is Health Care Mfg., Inc.. It received FDA 510(k) clearance on 2002-10-22 under 510(k) number K022737. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC?

HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC is a medical device that received FDA 510(k) clearance on 2002-10-22. The listed applicant is Health Care Mfg., Inc.. The 510(k) number is K022737.

When did HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC receive FDA 510(k) clearance?

HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC received FDA 510(k) clearance on 2002-10-22, under 510(k) number K022737.

Who is the listed applicant for HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC?

The FDA 510(k) record lists Health Care Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC?

The FDA product code for HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC is KPR.

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Other records listing Health Care Mfg., Inc. 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.

K022667HCMI X-RAYK952441LEGENDK951323VH-2000K951382HLT 406K944699ATT-300K944329BACK SPECIALIST

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Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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