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FDA 510(k)

HYPERSTETHOSCOPE, MODEL Z 00

K-Number: K801165 · 1980-05-23

ApplicantDemonbinder Electronics
Decision Date1980-05-23
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HYPERSTETHOSCOPE, MODEL Z 00 is the device name listed in this FDA 510(k) record. The listed applicant is Demonbinder Electronics. It received FDA 510(k) clearance on 1980-05-23 under 510(k) number K801165. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPERSTETHOSCOPE, MODEL Z 00?

HYPERSTETHOSCOPE, MODEL Z 00 is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Demonbinder Electronics. The 510(k) number is K801165.

When did HYPERSTETHOSCOPE, MODEL Z 00 receive FDA 510(k) clearance?

HYPERSTETHOSCOPE, MODEL Z 00 received FDA 510(k) clearance on 1980-05-23, under 510(k) number K801165.

Who is the listed applicant for HYPERSTETHOSCOPE, MODEL Z 00?

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

What is the FDA product code for HYPERSTETHOSCOPE, MODEL Z 00?

The FDA product code for HYPERSTETHOSCOPE, MODEL Z 00 is DQD.

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Related Devices (Code: DQD)

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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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