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FDA 510(k)

MVP (MULTI-VENDOR PROTOCOL CONVERTOR)

K-Number: K900227 · 1990-02-12

ApplicantMerge Technologies, Inc.
Decision Date1990-02-12
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MVP (MULTI-VENDOR PROTOCOL CONVERTOR) is the device name listed in this FDA 510(k) record. The listed applicant is Merge Technologies, Inc.. It received FDA 510(k) clearance on 1990-02-12 under 510(k) number K900227. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVP (MULTI-VENDOR PROTOCOL CONVERTOR)?

MVP (MULTI-VENDOR PROTOCOL CONVERTOR) is a medical device that received FDA 510(k) clearance on 1990-02-12. The listed applicant is Merge Technologies, Inc.. The 510(k) number is K900227.

When did MVP (MULTI-VENDOR PROTOCOL CONVERTOR) receive FDA 510(k) clearance?

MVP (MULTI-VENDOR PROTOCOL CONVERTOR) received FDA 510(k) clearance on 1990-02-12, under 510(k) number K900227.

Who is the listed applicant for MVP (MULTI-VENDOR PROTOCOL CONVERTOR)?

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

What is the FDA product code for MVP (MULTI-VENDOR PROTOCOL CONVERTOR)?

The FDA product code for MVP (MULTI-VENDOR PROTOCOL CONVERTOR) is LMD.

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Related Devices (Code: LMD)

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

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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