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FDA 510(k)

HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS

K-Number: K855150 · 1986-04-01

ApplicantHpk International, Inc.
Decision Date1986-04-01
Product CodeLKX
DecisionSubstantially Equivalent

Device Summary

HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS is the device name listed in this FDA 510(k) record. The listed applicant is Hpk International, Inc.. It received FDA 510(k) clearance on 1986-04-01 under 510(k) number K855150. The device is classified under product code LKX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS?

HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS is a medical device that received FDA 510(k) clearance on 1986-04-01. The listed applicant is Hpk International, Inc.. The 510(k) number is K855150.

When did HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS receive FDA 510(k) clearance?

HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS received FDA 510(k) clearance on 1986-04-01, under 510(k) number K855150.

Who is the listed applicant for HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS?

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

What is the FDA product code for HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS?

The FDA product code for HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS is LKX.

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Related Devices (Code: LKX)

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.

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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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