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FDA 510(k)

IMAX PERIOTIPS

K-Number: K851841 · 1985-05-29

ApplicantStram Dental, Inc.
Decision Date1985-05-29
Product Code
DecisionSubstantially Equivalent

Device Summary

IMAX PERIOTIPS is the device name listed in this FDA 510(k) record. The listed applicant is Stram Dental, Inc.. It received FDA 510(k) clearance on 1985-05-29 under 510(k) number K851841. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAX PERIOTIPS?

IMAX PERIOTIPS is a medical device that received FDA 510(k) clearance on 1985-05-29. The listed applicant is Stram Dental, Inc.. The 510(k) number is K851841.

When did IMAX PERIOTIPS receive FDA 510(k) clearance?

IMAX PERIOTIPS received FDA 510(k) clearance on 1985-05-29, under 510(k) number K851841.

Who is the listed applicant for IMAX PERIOTIPS?

The FDA 510(k) record lists Stram Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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