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FDA 510(k)

CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD

K-Number: K861019 · 1986-04-02

ApplicantPhase One Disign Co.
Decision Date1986-04-02
Product CodeEAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Phase One Disign Co.. It received FDA 510(k) clearance on 1986-04-02 under 510(k) number K861019. The device is classified under product code EAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD?

CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD is a medical device that received FDA 510(k) clearance on 1986-04-02. The listed applicant is Phase One Disign Co.. The 510(k) number is K861019.

When did CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD receive FDA 510(k) clearance?

CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD received FDA 510(k) clearance on 1986-04-02, under 510(k) number K861019.

Who is the listed applicant for CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD?

The FDA 510(k) record lists Phase One Disign Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD?

The FDA product code for CEILING MOUNT COUNTERPOISED SECON RADIATION SHIELD is EAK.

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Related Devices (Code: EAK)

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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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