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FDA 510(k)

SURGERY DISPLAY SYSTEM

K-Number: K800488 · 1980-04-16

ApplicantKent Barker & Assoc.
Decision Date1980-04-16
Product CodeDRQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SURGERY DISPLAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Kent Barker & Assoc.. It received FDA 510(k) clearance on 1980-04-16 under 510(k) number K800488. The device is classified under product code DRQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGERY DISPLAY SYSTEM?

SURGERY DISPLAY SYSTEM is a medical device that received FDA 510(k) clearance on 1980-04-16. The listed applicant is Kent Barker & Assoc.. The 510(k) number is K800488.

When did SURGERY DISPLAY SYSTEM receive FDA 510(k) clearance?

SURGERY DISPLAY SYSTEM received FDA 510(k) clearance on 1980-04-16, under 510(k) number K800488.

Who is the listed applicant for SURGERY DISPLAY SYSTEM?

The FDA 510(k) record lists Kent Barker & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGERY DISPLAY SYSTEM?

The FDA product code for SURGERY DISPLAY SYSTEM is DRQ.

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Related Devices (Code: DRQ)

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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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