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FDA 510(k)

MEDICOR QUALITY CONTROL BUFFER

K-Number: K791287 · 1979-08-16

ApplicantMedicor USA , Ltd.
Decision Date1979-08-16
Product CodeJJS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MEDICOR QUALITY CONTROL BUFFER is the device name listed in this FDA 510(k) record. The listed applicant is Medicor USA , Ltd.. It received FDA 510(k) clearance on 1979-08-16 under 510(k) number K791287. The device is classified under product code JJS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICOR QUALITY CONTROL BUFFER?

MEDICOR QUALITY CONTROL BUFFER is a medical device that received FDA 510(k) clearance on 1979-08-16. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K791287.

When did MEDICOR QUALITY CONTROL BUFFER receive FDA 510(k) clearance?

MEDICOR QUALITY CONTROL BUFFER received FDA 510(k) clearance on 1979-08-16, under 510(k) number K791287.

Who is the listed applicant for MEDICOR QUALITY CONTROL BUFFER?

The FDA 510(k) record lists Medicor USA , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDICOR QUALITY CONTROL BUFFER?

The FDA product code for MEDICOR QUALITY CONTROL BUFFER is JJS.

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Other records listing Medicor USA , Ltd. as applicant

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Related Devices (Code: JJS)

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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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