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FDA 510(k)

DEVICE FOR THE TREATMENT OF HEMORRHOIDS

K-Number: K822649 · 1982-11-03

ApplicantDunmore Corp.
Decision Date1982-11-03
Product CodeLKX
DecisionSubstantially Equivalent

Device Summary

DEVICE FOR THE TREATMENT OF HEMORRHOIDS is the device name listed in this FDA 510(k) record. The listed applicant is Dunmore Corp.. It received FDA 510(k) clearance on 1982-11-03 under 510(k) number K822649. The device is classified under product code LKX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVICE FOR THE TREATMENT OF HEMORRHOIDS?

DEVICE FOR THE TREATMENT OF HEMORRHOIDS is a medical device that received FDA 510(k) clearance on 1982-11-03. The listed applicant is Dunmore Corp.. The 510(k) number is K822649.

When did DEVICE FOR THE TREATMENT OF HEMORRHOIDS receive FDA 510(k) clearance?

DEVICE FOR THE TREATMENT OF HEMORRHOIDS received FDA 510(k) clearance on 1982-11-03, under 510(k) number K822649.

Who is the listed applicant for DEVICE FOR THE TREATMENT OF HEMORRHOIDS?

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

What is the FDA product code for DEVICE FOR THE TREATMENT OF HEMORRHOIDS?

The FDA product code for DEVICE FOR THE TREATMENT OF HEMORRHOIDS is LKX.

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.

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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.

K172358InstaliefPrivi Medical Pte, Ltd.K113660COLD PACK, PLASTIC APPLICATOR (MEDICAL GRADE)-NON-CHEMICALCryotherapy Products, Inc.K072414CRYOSTATLil Drug Store Products, Inc.K042564HEMOR-RITE CRYOTHERAPHYFama Holdings International CorpK012746ICE BATONBehive, Ltd.K981428ANU ICECryoptherapy Pain Relief Products, Inc.

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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