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FDA 510(k)

EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR

K-Number: K870851 · 1987-03-20

Decision Date1987-03-20
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Electromed Intl., Ltd.. It received FDA 510(k) clearance on 1987-03-20 under 510(k) number K870851. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR?

EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR is a medical device that received FDA 510(k) clearance on 1987-03-20. The listed applicant is Electromed Intl., Ltd.. The 510(k) number is K870851.

When did EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR receive FDA 510(k) clearance?

EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR received FDA 510(k) clearance on 1987-03-20, under 510(k) number K870851.

Who is the listed applicant for EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR?

The FDA 510(k) record lists Electromed Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR?

The FDA product code for EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR is IZO.

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.

Other records listing Electromed Intl., Ltd. 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.

View all 23 devices →

Related Devices (Code: IZO)

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.

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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