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FDA 510(k)

ZEROID HEMORRHOIDAL DEVICE

K-Number: K944874 · 1995-08-07

ApplicantMedical Appliance Research Corp.
Decision Date1995-08-07
Product CodeLKX
DecisionSubstantially Equivalent

Device Summary

ZEROID HEMORRHOIDAL DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Appliance Research Corp.. It received FDA 510(k) clearance on 1995-08-07 under 510(k) number K944874. The device is classified under product code LKX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEROID HEMORRHOIDAL DEVICE?

ZEROID HEMORRHOIDAL DEVICE is a medical device that received FDA 510(k) clearance on 1995-08-07. The listed applicant is Medical Appliance Research Corp.. The 510(k) number is K944874.

When did ZEROID HEMORRHOIDAL DEVICE receive FDA 510(k) clearance?

ZEROID HEMORRHOIDAL DEVICE received FDA 510(k) clearance on 1995-08-07, under 510(k) number K944874.

Who is the listed applicant for ZEROID HEMORRHOIDAL DEVICE?

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

What is the FDA product code for ZEROID HEMORRHOIDAL DEVICE?

The FDA product code for ZEROID HEMORRHOIDAL DEVICE 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.

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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