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FDA 510(k)

PIO ROOT CANAL INDICATOR

K-Number: K822793 · 1982-10-22

ApplicantNational Patent Development Corp.
Decision Date1982-10-22
Product CodeEIL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PIO ROOT CANAL INDICATOR 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 1982-10-22 under 510(k) number K822793. The device is classified under product code EIL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIO ROOT CANAL INDICATOR?

PIO ROOT CANAL INDICATOR is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is National Patent Development Corp.. The 510(k) number is K822793.

When did PIO ROOT CANAL INDICATOR receive FDA 510(k) clearance?

PIO ROOT CANAL INDICATOR received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822793.

Who is the listed applicant for PIO ROOT CANAL INDICATOR?

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 PIO ROOT CANAL INDICATOR?

The FDA product code for PIO ROOT CANAL INDICATOR is EIL.

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Other records listing National Patent Development Corp. as applicant

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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Related Devices (Code: EIL)

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.

K911643ABIODENT PERIOTEMP(R) SYSTEMAbiomed, Inc.K890493FLORIDA PROBE PERIODONTAL PROBEFlorida Probe Corp.K885075ABIOMED PERIOTEMP(TM) PROBEAbiomed, Inc.K884813MODEL 200A ELECTRONIC FORCE-SENSING PROBEVine Valley ResearchK880209PERIODONTAL PROBE - AUTOPROBEDentsply Intl.K872098CREMEEN ALVEOLAR BONE CALIPERBowen & Company, Inc.

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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