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FDA 510(k)

PLAN-32 SOFTWARE

K-Number: K871810 · 1987-10-30

ApplicantOncology Systems, Inc.
Decision Date1987-10-30
Product CodeJAD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PLAN-32 SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Oncology Systems, Inc.. It received FDA 510(k) clearance on 1987-10-30 under 510(k) number K871810. 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 PLAN-32 SOFTWARE?

PLAN-32 SOFTWARE is a medical device that received FDA 510(k) clearance on 1987-10-30. The listed applicant is Oncology Systems, Inc.. The 510(k) number is K871810.

When did PLAN-32 SOFTWARE receive FDA 510(k) clearance?

PLAN-32 SOFTWARE received FDA 510(k) clearance on 1987-10-30, under 510(k) number K871810.

Who is the listed applicant for PLAN-32 SOFTWARE?

The FDA 510(k) record lists Oncology Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLAN-32 SOFTWARE?

The FDA product code for PLAN-32 SOFTWARE is JAD.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Oncology Systems, Inc. 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.

K123357ONQ RTSK092522ACU007SK051753ACCU-SOURCE

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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