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FDA 510(k)

DISPOPROPHY

K-Number: K993182 · 2001-08-06

ApplicantKis Products
Decision Date2001-08-06
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISPOPROPHY is the device name listed in this FDA 510(k) record. The listed applicant is Kis Products. It received FDA 510(k) clearance on 2001-08-06 under 510(k) number K993182. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOPROPHY?

DISPOPROPHY is a medical device that received FDA 510(k) clearance on 2001-08-06. The listed applicant is Kis Products. The 510(k) number is K993182.

When did DISPOPROPHY receive FDA 510(k) clearance?

DISPOPROPHY received FDA 510(k) clearance on 2001-08-06, under 510(k) number K993182.

Who is the listed applicant for DISPOPROPHY?

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

What is the FDA product code for DISPOPROPHY?

The FDA product code for DISPOPROPHY is KOJ.

Related Clinical Trials

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.

Other records listing Kis Products 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.

Related Devices (Code: KOJ)

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.

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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