FDA 510(k)

DRY TIPS

K-Number: K890734 · 1989-03-10

Decision Date1989-03-10

Product CodeKHR

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DRY TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Microcopy, Div. Neo-Flo, Inc.. It received FDA 510(k) clearance on 1989-03-10 under 510(k) number K890734. The device is classified under product code KHR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRY TIPS?

DRY TIPS is a medical device that received FDA 510(k) clearance on 1989-03-10. The listed applicant is Microcopy, Div. Neo-Flo, Inc.. The 510(k) number is K890734.

When did DRY TIPS receive FDA 510(k) clearance?

DRY TIPS received FDA 510(k) clearance on 1989-03-10, under 510(k) number K890734.

Who is the listed applicant for DRY TIPS?

The FDA 510(k) record lists Microcopy, Div. Neo-Flo, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRY TIPS?

The FDA product code for DRY TIPS is KHR.

Other records listing Microcopy, Div. Neo-Flo, Inc. as applicant

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.

K885233NOVA DIAMOND

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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.