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FDA 510(k)

AUTO-RINSE

K-Number: K770152 · 1977-01-31

ApplicantDental Innovators, Inc.
Decision Date1977-01-31
Product CodeEHZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AUTO-RINSE is the device name listed in this FDA 510(k) record. The listed applicant is Dental Innovators, Inc.. It received FDA 510(k) clearance on 1977-01-31 under 510(k) number K770152. The device is classified under product code EHZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-RINSE?

AUTO-RINSE is a medical device that received FDA 510(k) clearance on 1977-01-31. The listed applicant is Dental Innovators, Inc.. The 510(k) number is K770152.

When did AUTO-RINSE receive FDA 510(k) clearance?

AUTO-RINSE received FDA 510(k) clearance on 1977-01-31, under 510(k) number K770152.

Who is the listed applicant for AUTO-RINSE?

The FDA 510(k) record lists Dental Innovators, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO-RINSE?

The FDA product code for AUTO-RINSE is EHZ.

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Related Devices (Code: EHZ)

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.

K973248IMTEC BONE COLLECTOR SYSTEMImtec Corp.K941164TAP EXPRESS EJECTORTap Express, Inc.K911072SUPER EVACRETRACTOR, DISPOSABLE ORAL EVACUATORA & F ProductsK903718OROSCOPE MODEL NUMBER COS-100Cygnus Instruments, Inc.K892881DENTAL SANI-SLEEVE STERILE 60MM X 1650MM #1101Nieusma R & D, Inc.K892882DENTAL SANI-SLEEVE STERILE 100MM X 2200MM #1102Nieusma R & D, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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