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FDA 510(k)

MVP - 6000

K-Number: K852909 · 1985-11-14

ApplicantWaters Instruments, Inc.
Decision Date1985-11-14
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MVP - 6000 is the device name listed in this FDA 510(k) record. The listed applicant is Waters Instruments, Inc.. It received FDA 510(k) clearance on 1985-11-14 under 510(k) number K852909. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVP - 6000?

MVP - 6000 is a medical device that received FDA 510(k) clearance on 1985-11-14. The listed applicant is Waters Instruments, Inc.. The 510(k) number is K852909.

When did MVP - 6000 receive FDA 510(k) clearance?

MVP - 6000 received FDA 510(k) clearance on 1985-11-14, under 510(k) number K852909.

Who is the listed applicant for MVP - 6000?

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

What is the FDA product code for MVP - 6000?

The FDA product code for MVP - 6000 is BZC.

Other records listing Waters Instruments, Inc. as applicant

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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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