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FDA 510(k)

AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM

K-Number: K974239 · 1998-02-10

Decision Date1998-02-10
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aktina Medical Physics Corp.. It received FDA 510(k) clearance on 1998-02-10 under 510(k) number K974239. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM?

AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM is a medical device that received FDA 510(k) clearance on 1998-02-10. The listed applicant is Aktina Medical Physics Corp.. The 510(k) number is K974239.

When did AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM receive FDA 510(k) clearance?

AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM received FDA 510(k) clearance on 1998-02-10, under 510(k) number K974239.

Who is the listed applicant for AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM?

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

What is the FDA product code for AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM?

The FDA product code for AKTINA MEDICAL PHYSICS CORPORATION PHOTON BEAM BLOCKING SYSTEM is IXI.

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 Aktina Medical Physics 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.

View all 13 devices →

Related Devices (Code: IXI)

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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