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FDA 510(k)

PROGRAMMABLE PATIENT SIMULATOR

K-Number: K844464 · 1985-04-03

ApplicantRamford Labs
Decision Date1985-04-03
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PROGRAMMABLE PATIENT SIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ramford Labs. It received FDA 510(k) clearance on 1985-04-03 under 510(k) number K844464. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROGRAMMABLE PATIENT SIMULATOR?

PROGRAMMABLE PATIENT SIMULATOR is a medical device that received FDA 510(k) clearance on 1985-04-03. The listed applicant is Ramford Labs. The 510(k) number is K844464.

When did PROGRAMMABLE PATIENT SIMULATOR receive FDA 510(k) clearance?

PROGRAMMABLE PATIENT SIMULATOR received FDA 510(k) clearance on 1985-04-03, under 510(k) number K844464.

Who is the listed applicant for PROGRAMMABLE PATIENT SIMULATOR?

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

What is the FDA product code for PROGRAMMABLE PATIENT SIMULATOR?

The FDA product code for PROGRAMMABLE PATIENT SIMULATOR is DSI.

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Related Devices (Code: DSI)

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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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