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FDA 510(k)

MERSHON BAND PUSHER

K-Number: K935155 · 1994-02-04

ApplicantDentauraum, Inc.
Decision Date1994-02-04
Product CodeECS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MERSHON BAND PUSHER is the device name listed in this FDA 510(k) record. The listed applicant is Dentauraum, Inc.. It received FDA 510(k) clearance on 1994-02-04 under 510(k) number K935155. The device is classified under product code ECS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERSHON BAND PUSHER?

MERSHON BAND PUSHER is a medical device that received FDA 510(k) clearance on 1994-02-04. The listed applicant is Dentauraum, Inc.. The 510(k) number is K935155.

When did MERSHON BAND PUSHER receive FDA 510(k) clearance?

MERSHON BAND PUSHER received FDA 510(k) clearance on 1994-02-04, under 510(k) number K935155.

Who is the listed applicant for MERSHON BAND PUSHER?

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 MERSHON BAND PUSHER?

The FDA product code for MERSHON BAND PUSHER is ECS.

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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

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Related Devices (Code: ECS)

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.

K924993GLENROE BAND SEATING CONTOURING INSTRUMENTGlenroe Technologies

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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