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FDA 510(k)

RTP-5000

K-Number: K813439 · 1982-01-22

ApplicantAdac Laboratories
Decision Date1982-01-22
Product CodeJAD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RTP-5000 is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K813439. The device is classified under product code JAD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RTP-5000?

RTP-5000 is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Adac Laboratories. The 510(k) number is K813439.

When did RTP-5000 receive FDA 510(k) clearance?

RTP-5000 received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813439.

Who is the listed applicant for RTP-5000?

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

What is the FDA product code for RTP-5000?

The FDA product code for RTP-5000 is JAD.

Other records listing Adac Laboratories 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: JAD)

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.

K250692GentleBeam (GB1000)Voxel Ray Solutions, LLCK241174INTRABEAM (700); And accessories (INTRABEAM SMART Stand, INTRABEAM SMART Spherical Applicator, INTRABEAM Spherical Sizer Set, INTRABEAM Needle Applicator)Carl Zeiss Meditec, AGK230611X80 / RADiant / PhotoElectric Therapy System (RADiant Aura)Xstrahl, Ltd.K213942EsteyaNucletron B.V.K190255Sensus Healthcare TVM Balloon ApplicatorSensus Healthcare, Inc.K182641Sensus IORT SystemSensus Healthcare, Inc.

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.

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