FDA 510(k)

AKTINA MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER

K-Number: K990997 · 1999-06-22

Decision Date1999-06-22

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

AKTINA MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER 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 1999-06-22 under 510(k) number K990997. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AKTINA MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER?

AKTINA MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER is a medical device that received FDA 510(k) clearance on 1999-06-22. The listed applicant is Aktina Medical Physics Corp.. The 510(k) number is K990997.

When did AKTINA MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER receive FDA 510(k) clearance?

AKTINA MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER received FDA 510(k) clearance on 1999-06-22, under 510(k) number K990997.

Who is the listed applicant for AKTINA MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER?

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 MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER?

The FDA product code for AKTINA MEDICALPHYSICS CORPORATION MECHANICAL FRONTPOINTER is IYE.

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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.