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FDA 510(k)

PERIO PIK

K-Number: K840721 · 1984-04-25

ApplicantTeledyne, Inc.
Decision Date1984-04-25
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIO PIK is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne, Inc.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K840721. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIO PIK?

PERIO PIK is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Teledyne, Inc.. The 510(k) number is K840721.

When did PERIO PIK receive FDA 510(k) clearance?

PERIO PIK received FDA 510(k) clearance on 1984-04-25, under 510(k) number K840721.

Who is the listed applicant for PERIO PIK?

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

What is the FDA product code for PERIO PIK?

The FDA product code for PERIO PIK is EFS.

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Other records listing Teledyne, Inc. as applicant

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Related Devices (Code: EFS)

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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