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FDA 510(k)

DNA MEDICAL DURACATH

K-Number: K822436 · 1982-10-22

ApplicantMoorehead Hospital Products, Inc.
Decision Date1982-10-22
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DNA MEDICAL DURACATH is the device name listed in this FDA 510(k) record. The listed applicant is Moorehead Hospital Products, Inc.. It received FDA 510(k) clearance on 1982-10-22 under 510(k) number K822436. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DNA MEDICAL DURACATH?

DNA MEDICAL DURACATH is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is Moorehead Hospital Products, Inc.. The 510(k) number is K822436.

When did DNA MEDICAL DURACATH receive FDA 510(k) clearance?

DNA MEDICAL DURACATH received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822436.

Who is the listed applicant for DNA MEDICAL DURACATH?

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

What is the FDA product code for DNA MEDICAL DURACATH?

The FDA product code for DNA MEDICAL DURACATH is BSO.

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Related Devices (Code: BSO)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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