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Plan-32 Software

by Oncology Systems, Inc.

510(k) K871810

Plan-32 Software is a medical device (FDA Class II; FDA product code JAD, System, Therapeutic, X-Ray) made by Oncology Systems, Inc., cleared under FDA 510(k) K871810 on 30 Oct 1987, active as of 9 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 9 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 9 Oct 2026.

Regulatory status

as of registry sync 9 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK871810 Date30 Oct 1987ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
JAD
Device class
Class II
Regulation
21 CFR Part 892.5900
Advisory committee
Radiology
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code JAD (System, Therapeutic, X-Ray).

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