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FDA 510(k)

CATHETER, MEDIASTINAL&PERICARDIAL

K-Number: K771986 · 1977-10-28

ApplicantThe Minnesota Back Brace Co.
Decision Date1977-10-28
Product CodeFHF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER, MEDIASTINAL&PERICARDIAL is the device name listed in this FDA 510(k) record. The listed applicant is The Minnesota Back Brace Co.. It received FDA 510(k) clearance on 1977-10-28 under 510(k) number K771986. The device is classified under product code FHF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER, MEDIASTINAL&PERICARDIAL?

CATHETER, MEDIASTINAL&PERICARDIAL is a medical device that received FDA 510(k) clearance on 1977-10-28. The listed applicant is The Minnesota Back Brace Co.. The 510(k) number is K771986.

When did CATHETER, MEDIASTINAL&PERICARDIAL receive FDA 510(k) clearance?

CATHETER, MEDIASTINAL&PERICARDIAL received FDA 510(k) clearance on 1977-10-28, under 510(k) number K771986.

Who is the listed applicant for CATHETER, MEDIASTINAL&PERICARDIAL?

The FDA 510(k) record lists The Minnesota Back Brace Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER, MEDIASTINAL&PERICARDIAL?

The FDA product code for CATHETER, MEDIASTINAL&PERICARDIAL is FHF.

Related Clinical Trials

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Related Devices (Code: FHF)

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.

K093479DISPOSABLE SUCTION AND IRRIGATION SYSTEMModern Medical Equipment Mfg., Ltd.K003443SUCTION IRRIGATORApplied Medical

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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