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FDA 510(k)

PERMA-PIC PLASTIC TOOTHPICK

K-Number: K881900 · 1988-06-01

Decision Date1988-06-01
Product CodeJET
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERMA-PIC PLASTIC TOOTHPICK is the device name listed in this FDA 510(k) record. The listed applicant is The Perma-Pic Co.. It received FDA 510(k) clearance on 1988-06-01 under 510(k) number K881900. The device is classified under product code JET. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERMA-PIC PLASTIC TOOTHPICK?

PERMA-PIC PLASTIC TOOTHPICK is a medical device that received FDA 510(k) clearance on 1988-06-01. The listed applicant is The Perma-Pic Co.. The 510(k) number is K881900.

When did PERMA-PIC PLASTIC TOOTHPICK receive FDA 510(k) clearance?

PERMA-PIC PLASTIC TOOTHPICK received FDA 510(k) clearance on 1988-06-01, under 510(k) number K881900.

Who is the listed applicant for PERMA-PIC PLASTIC TOOTHPICK?

The FDA 510(k) record lists The Perma-Pic Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERMA-PIC PLASTIC TOOTHPICK?

The FDA product code for PERMA-PIC PLASTIC TOOTHPICK is JET.

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.

Related Devices (Code: JET)

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.

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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