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FDA 510(k)

H-TYPE BRIDGE REMOVER

K-Number: K842026 · 1984-07-11

ApplicantHiga Manufacturing , Ltd.
Decision Date1984-07-11
Product CodeEIS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

H-TYPE BRIDGE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Higa Manufacturing , Ltd.. It received FDA 510(k) clearance on 1984-07-11 under 510(k) number K842026. The device is classified under product code EIS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H-TYPE BRIDGE REMOVER?

H-TYPE BRIDGE REMOVER is a medical device that received FDA 510(k) clearance on 1984-07-11. The listed applicant is Higa Manufacturing , Ltd.. The 510(k) number is K842026.

When did H-TYPE BRIDGE REMOVER receive FDA 510(k) clearance?

H-TYPE BRIDGE REMOVER received FDA 510(k) clearance on 1984-07-11, under 510(k) number K842026.

Who is the listed applicant for H-TYPE BRIDGE REMOVER?

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

What is the FDA product code for H-TYPE BRIDGE REMOVER?

The FDA product code for H-TYPE BRIDGE REMOVER is EIS.

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Related Devices (Code: EIS)

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.

K992649ATD AUTOMATIC BRIDGE REMOVERJ. Morita USA, Inc.K951299EASY PNEUMATIC CROWN AND BRIDGE REMOVERDentco, Inc.K863500STAINLESS STEEL DEN. CROWN REMOVER & AMA./COMP.CARPacific Union Dental, Inc.K854795HAZELTON TEMPORARY CROWN AND BRIDGE REMOVERFran Hazelton Co.K833287SATIN CAST ECONOCASTGenesis Industries, Inc.K833290C & B 40 PENTRO C & B40Genesis Industries, 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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