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FDA 510(k)

DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS

K-Number: K935156 · 1994-02-03

ApplicantDentauraum, Inc.
Decision Date1994-02-03
Product CodeECR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Dentauraum, Inc.. It received FDA 510(k) clearance on 1994-02-03 under 510(k) number K935156. The device is classified under product code ECR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS?

DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-02-03. The listed applicant is Dentauraum, Inc.. The 510(k) number is K935156.

When did DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS receive FDA 510(k) clearance?

DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS received FDA 510(k) clearance on 1994-02-03, under 510(k) number K935156.

Who is the listed applicant for DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS?

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

What is the FDA product code for DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS?

The FDA product code for DENTAURUM BAND SEATER AND BAND SEATING INSTRUMENTS is ECR.

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Other records listing Dentauraum, Inc. 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.

K952867REMANIUM:GM 700, GM 380, GM 800, GFHK952866REMATITAN TITANIUMK952870REMANIUM: CS & G-SOFTK952865REMANIUM: 200,CS, 380, AND CDK952868DENTAURUM JACKET CROWN & ROOT POSTSK942667DENT-O-CRYL ORTHODONTIC ACRYLIC

View all 24 devices →

Related Devices (Code: ECR)

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.

K951776BAND SEATEROrmco Corp.K843018FLEXI-POSTEssential Dental Systems, 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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