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FDA 510(k)

ENDOGATOR

K-Number: K770813 · 1977-05-20

ApplicantAus-Tex Dental Mfg. & Design
Decision Date1977-05-20
Product CodeEIC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Aus-Tex Dental Mfg. & Design. It received FDA 510(k) clearance on 1977-05-20 under 510(k) number K770813. 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 ENDOGATOR?

ENDOGATOR is a medical device that received FDA 510(k) clearance on 1977-05-20. The listed applicant is Aus-Tex Dental Mfg. & Design. The 510(k) number is K770813.

When did ENDOGATOR receive FDA 510(k) clearance?

ENDOGATOR received FDA 510(k) clearance on 1977-05-20, under 510(k) number K770813.

Who is the listed applicant for ENDOGATOR?

The FDA 510(k) record lists Aus-Tex Dental Mfg. & Design as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOGATOR?

The FDA product code for ENDOGATOR is EIC.

Related Clinical Trials

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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Other records listing Aus-Tex Dental Mfg. & Design 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.

K811594WATER PISTOLK771406GUTTA GUN

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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