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FDA 510(k)

MODEL 4100 14 MEV NEUTRON GEN. THERAPY

K-Number: K811778 · 1981-07-23

Decision Date1981-07-23
Product CodeIWL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 4100 14 MEV NEUTRON GEN. THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is The Cyclotron Corp.. It received FDA 510(k) clearance on 1981-07-23 under 510(k) number K811778. The device is classified under product code IWL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 4100 14 MEV NEUTRON GEN. THERAPY?

MODEL 4100 14 MEV NEUTRON GEN. THERAPY is a medical device that received FDA 510(k) clearance on 1981-07-23. The listed applicant is The Cyclotron Corp.. The 510(k) number is K811778.

When did MODEL 4100 14 MEV NEUTRON GEN. THERAPY receive FDA 510(k) clearance?

MODEL 4100 14 MEV NEUTRON GEN. THERAPY received FDA 510(k) clearance on 1981-07-23, under 510(k) number K811778.

Who is the listed applicant for MODEL 4100 14 MEV NEUTRON GEN. THERAPY?

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

What is the FDA product code for MODEL 4100 14 MEV NEUTRON GEN. THERAPY?

The FDA product code for MODEL 4100 14 MEV NEUTRON GEN. THERAPY is IWL.

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 The Cyclotron Corp. 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.

Related Devices (Code: IWL)

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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