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FDA 510(k)

ZONOGRAPH 6

K-Number: K810307 · 1981-03-11

ApplicantSiemens Corp.
Decision Date1981-03-11
Product CodeIZF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ZONOGRAPH 6 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1981-03-11 under 510(k) number K810307. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZONOGRAPH 6?

ZONOGRAPH 6 is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is Siemens Corp.. The 510(k) number is K810307.

When did ZONOGRAPH 6 receive FDA 510(k) clearance?

ZONOGRAPH 6 received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810307.

Who is the listed applicant for ZONOGRAPH 6?

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

What is the FDA product code for ZONOGRAPH 6?

The FDA product code for ZONOGRAPH 6 is IZF.

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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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