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FDA 510(k)

COMPUTE RX-PLAN

K-Number: K850977 · 1985-07-26

ApplicantMedicalibration
Decision Date1985-07-26
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMPUTE RX-PLAN is the device name listed in this FDA 510(k) record. The listed applicant is Medicalibration. It received FDA 510(k) clearance on 1985-07-26 under 510(k) number K850977. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUTE RX-PLAN?

COMPUTE RX-PLAN is a medical device that received FDA 510(k) clearance on 1985-07-26. The listed applicant is Medicalibration. The 510(k) number is K850977.

When did COMPUTE RX-PLAN receive FDA 510(k) clearance?

COMPUTE RX-PLAN received FDA 510(k) clearance on 1985-07-26, under 510(k) number K850977.

Who is the listed applicant for COMPUTE RX-PLAN?

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

What is the FDA product code for COMPUTE RX-PLAN?

The FDA product code for COMPUTE RX-PLAN is KPQ.

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Related Devices (Code: KPQ)

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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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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