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FDA 510(k)

FILE, PULP CANAL

K-Number: K800293 · 1980-02-19

ApplicantIpco Corp.
Decision Date1980-02-19
Product CodeEKS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FILE, PULP CANAL is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1980-02-19 under 510(k) number K800293. The device is classified under product code EKS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILE, PULP CANAL?

FILE, PULP CANAL is a medical device that received FDA 510(k) clearance on 1980-02-19. The listed applicant is Ipco Corp.. The 510(k) number is K800293.

When did FILE, PULP CANAL receive FDA 510(k) clearance?

FILE, PULP CANAL received FDA 510(k) clearance on 1980-02-19, under 510(k) number K800293.

Who is the listed applicant for FILE, PULP CANAL?

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

What is the FDA product code for FILE, PULP CANAL?

The FDA product code for FILE, PULP CANAL is EKS.

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Other records listing Ipco Corp. as applicant

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Related Devices (Code: EKS)

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.

K062856TF ROTARY NICKEL TITANIUM FILEOrmco Corp.K004031NT SWIFT; TI\TEC; GATES GLIDDEN DRILLS; DENTAL POWER ENDODONTIC HAND FILESDental Power, Inc.K971319NT SERIES ENDODONTIC FILES, MAC SERIES ENDODONTIC FILESTycom DentalK970649HERO 642Micro-MegaK962031QUANTEC SERIES 2000 ENDODONTIC FILESTycom DentalK953604SHAPING HEDSTROM N.T.Sybron Dental Specialties, 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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