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FDA 510(k)

ROOT CANAL FILLING APPLICATOR NEEDLES

K-Number: K801484 · 1980-07-21

ApplicantNational Patent Development Corp.
Decision Date1980-07-21
Product CodeEIC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ROOT CANAL FILLING APPLICATOR NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K801484. The device is classified under product code EIC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROOT CANAL FILLING APPLICATOR NEEDLES?

ROOT CANAL FILLING APPLICATOR NEEDLES is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is National Patent Development Corp.. The 510(k) number is K801484.

When did ROOT CANAL FILLING APPLICATOR NEEDLES receive FDA 510(k) clearance?

ROOT CANAL FILLING APPLICATOR NEEDLES received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801484.

Who is the listed applicant for ROOT CANAL FILLING APPLICATOR NEEDLES?

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROOT CANAL FILLING APPLICATOR NEEDLES?

The FDA product code for ROOT CANAL FILLING APPLICATOR NEEDLES is EIC.

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Other records listing National Patent Development Corp. as applicant

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K843974VARIABLE TEMPERATURE CAUTERY DEVICEK832699HYDRON WOUND DRESSING FAST SEAT KITK822793PIO ROOT CANAL INDICATORK820028ZEON COMPOSITE RESIN LIGHT CURE SYSK820006ZEON COMPOSITE RESIN SYSTEMK811446HYDRON WOUND DRESSING KIT

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Related Devices (Code: EIC)

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.

K972234RCT GEL ROOT CANAL THERAPY GELDentsply Intl.K864307MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)Smith & Nephew, Inc.K861846HYDRON ROOT CANAL FILLING & MARK IV STARTER KITSolar Dental Co., Inc.K851944MAX-I-PROBE HANDPIECESolo Pak LaboratoriesK840237MAX-I-PROBE PERIODONTAL ENDODONTIC PROBSmith & Nephew, Mpl DivisionK811889R & S SERIES FITTING TOOLSSuncoast Dental Corp.

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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