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FDA 510(k)

MYOCATH CATOLOG NO. MCK-A

K-Number: K812052 · 1981-10-06

ApplicantSorensen Research
Decision Date1981-10-06
Product Code
DecisionSubstantially Equivalent

Device Summary

MYOCATH CATOLOG NO. MCK-A is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1981-10-06 under 510(k) number K812052. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYOCATH CATOLOG NO. MCK-A?

MYOCATH CATOLOG NO. MCK-A is a medical device that received FDA 510(k) clearance on 1981-10-06. The listed applicant is Sorensen Research. The 510(k) number is K812052.

When did MYOCATH CATOLOG NO. MCK-A receive FDA 510(k) clearance?

MYOCATH CATOLOG NO. MCK-A received FDA 510(k) clearance on 1981-10-06, under 510(k) number K812052.

Who is the listed applicant for MYOCATH CATOLOG NO. MCK-A?

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

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Other records listing Sorensen Research 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.

K833674ACCURATE MEASUREMENT DEVICE KG-AMDK833673ACCURATE MEASUREMENT DEVICE EZ-AMDK833095TRANSDUCER DOME SD105K833096TRANSDUCER DOME DS106K833094TRANSDUCER DOME SD104K832957FLOW-DIRECTED HEPARIN COATED THERMODIL

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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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