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FDA 510(k)

PORTA-PRO TOOTH POLISHER

K-Number: K770116 · 1977-01-28

ApplicantPorta-Pro, Inc.
Decision Date1977-01-28
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORTA-PRO TOOTH POLISHER is the device name listed in this FDA 510(k) record. The listed applicant is Porta-Pro, Inc.. It received FDA 510(k) clearance on 1977-01-28 under 510(k) number K770116. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTA-PRO TOOTH POLISHER?

PORTA-PRO TOOTH POLISHER is a medical device that received FDA 510(k) clearance on 1977-01-28. The listed applicant is Porta-Pro, Inc.. The 510(k) number is K770116.

When did PORTA-PRO TOOTH POLISHER receive FDA 510(k) clearance?

PORTA-PRO TOOTH POLISHER received FDA 510(k) clearance on 1977-01-28, under 510(k) number K770116.

Who is the listed applicant for PORTA-PRO TOOTH POLISHER?

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

What is the FDA product code for PORTA-PRO TOOTH POLISHER?

The FDA product code for PORTA-PRO TOOTH POLISHER is JEQ.

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Related Devices (Code: JEQ)

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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