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FDA 510(k)

NEW PER-FIT(R) IMPROVED

K-Number: K901621 · 1990-06-26

ApplicantDental Product Co.
Decision Date1990-06-26
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NEW PER-FIT(R) IMPROVED is the device name listed in this FDA 510(k) record. The listed applicant is Dental Product Co.. It received FDA 510(k) clearance on 1990-06-26 under 510(k) number K901621. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW PER-FIT(R) IMPROVED?

NEW PER-FIT(R) IMPROVED is a medical device that received FDA 510(k) clearance on 1990-06-26. The listed applicant is Dental Product Co.. The 510(k) number is K901621.

When did NEW PER-FIT(R) IMPROVED receive FDA 510(k) clearance?

NEW PER-FIT(R) IMPROVED received FDA 510(k) clearance on 1990-06-26, under 510(k) number K901621.

Who is the listed applicant for NEW PER-FIT(R) IMPROVED?

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

What is the FDA product code for NEW PER-FIT(R) IMPROVED?

The FDA product code for NEW PER-FIT(R) IMPROVED is EBI.

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Related Devices (Code: EBI)

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.

K261802Glidewell™ Denture Base ResinPrismatik Dentalcraft, Inc.K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, Inc.

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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