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FDA 510(k)

SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT

K-Number: K862029 · 1986-07-16

ApplicantElmed, Inc.
Decision Date1986-07-16
Product CodeIOA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Elmed, Inc.. It received FDA 510(k) clearance on 1986-07-16 under 510(k) number K862029. The device is classified under product code IOA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT?

SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT is a medical device that received FDA 510(k) clearance on 1986-07-16. The listed applicant is Elmed, Inc.. The 510(k) number is K862029.

When did SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT receive FDA 510(k) clearance?

SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT received FDA 510(k) clearance on 1986-07-16, under 510(k) number K862029.

Who is the listed applicant for SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT?

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

What is the FDA product code for SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT?

The FDA product code for SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNIT is IOA.

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 Elmed, 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.

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Related Devices (Code: IOA)

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

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

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