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FDA 510(k)

PERIOTEST

K-Number: K872171 · 1987-06-23

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1987-06-23
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIOTEST is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1987-06-23 under 510(k) number K872171. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIOTEST?

PERIOTEST is a medical device that received FDA 510(k) clearance on 1987-06-23. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K872171.

When did PERIOTEST receive FDA 510(k) clearance?

PERIOTEST received FDA 510(k) clearance on 1987-06-23, under 510(k) number K872171.

Who is the listed applicant for PERIOTEST?

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

What is the FDA product code for PERIOTEST?

The FDA product code for PERIOTEST is EKX.

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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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