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FDA 510(k)

DAIWA MODEL 180

K-Number: K983616 · 1999-10-15

ApplicantDaiwa Products, Inc.
Decision Date1999-10-15
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DAIWA MODEL 180 is the device name listed in this FDA 510(k) record. The listed applicant is Daiwa Products, Inc.. It received FDA 510(k) clearance on 1999-10-15 under 510(k) number K983616. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAIWA MODEL 180?

DAIWA MODEL 180 is a medical device that received FDA 510(k) clearance on 1999-10-15. The listed applicant is Daiwa Products, Inc.. The 510(k) number is K983616.

When did DAIWA MODEL 180 receive FDA 510(k) clearance?

DAIWA MODEL 180 received FDA 510(k) clearance on 1999-10-15, under 510(k) number K983616.

Who is the listed applicant for DAIWA MODEL 180?

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

What is the FDA product code for DAIWA MODEL 180?

The FDA product code for DAIWA MODEL 180 is DXN.

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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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