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FDA 510(k)

AMP DIRECT VASCULAR MONITORING SYSTEM

K-Number: K792646 · 1980-02-11

ApplicantAmerican Medical Products, Inc.
Decision Date1980-02-11
Product CodeKRH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMP DIRECT VASCULAR MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Products, Inc.. It received FDA 510(k) clearance on 1980-02-11 under 510(k) number K792646. The device is classified under product code KRH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMP DIRECT VASCULAR MONITORING SYSTEM?

AMP DIRECT VASCULAR MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1980-02-11. The listed applicant is American Medical Products, Inc.. The 510(k) number is K792646.

When did AMP DIRECT VASCULAR MONITORING SYSTEM receive FDA 510(k) clearance?

AMP DIRECT VASCULAR MONITORING SYSTEM received FDA 510(k) clearance on 1980-02-11, under 510(k) number K792646.

Who is the listed applicant for AMP DIRECT VASCULAR MONITORING SYSTEM?

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

What is the FDA product code for AMP DIRECT VASCULAR MONITORING SYSTEM?

The FDA product code for AMP DIRECT VASCULAR MONITORING SYSTEM is KRH.

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Other records listing American Medical Products, Inc. as applicant

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Related Devices (Code: KRH)

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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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