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FDA 510(k)

WATER PISTOL

K-Number: K811594 · 1981-07-15

ApplicantAus-Tex Dental Mfg. & Design
Decision Date1981-07-15
Product CodeEIC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WATER PISTOL 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 1981-07-15 under 510(k) number K811594. 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 WATER PISTOL?

WATER PISTOL is a medical device that received FDA 510(k) clearance on 1981-07-15. The listed applicant is Aus-Tex Dental Mfg. & Design. The 510(k) number is K811594.

When did WATER PISTOL receive FDA 510(k) clearance?

WATER PISTOL received FDA 510(k) clearance on 1981-07-15, under 510(k) number K811594.

Who is the listed applicant for WATER PISTOL?

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 WATER PISTOL?

The FDA product code for WATER PISTOL 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.

K771406GUTTA GUNK770813ENDOGATOR

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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