FDA 510(k)

MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.

K-Number: K871712 · 1988-01-14

Decision Date1988-01-14

Product CodeNVE

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT. is the device name listed in this FDA 510(k) record. The listed applicant is Machida America, Inc.. It received FDA 510(k) clearance on 1988-01-14 under 510(k) number K871712. The device is classified under product code NVE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.?

MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT. is a medical device that received FDA 510(k) clearance on 1988-01-14. The listed applicant is Machida America, Inc.. The 510(k) number is K871712.

When did MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT. receive FDA 510(k) clearance?

MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT. received FDA 510(k) clearance on 1988-01-14, under 510(k) number K871712.

Who is the listed applicant for MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.?

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

What is the FDA product code for MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.?

The FDA product code for MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT. is NVE.

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Other records listing Machida America, Inc. as applicant

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Related Devices (Code: NVE)

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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.