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FDA 510(k)

BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG

K-Number: K844554 · 1985-02-21

ApplicantBelmont Equipment Corp.
Decision Date1985-02-21
Product CodeIWZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG is the device name listed in this FDA 510(k) record. The listed applicant is Belmont Equipment Corp.. It received FDA 510(k) clearance on 1985-02-21 under 510(k) number K844554. The device is classified under product code IWZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG?

BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K844554.

When did BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG receive FDA 510(k) clearance?

BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG received FDA 510(k) clearance on 1985-02-21, under 510(k) number K844554.

Who is the listed applicant for BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG?

The FDA 510(k) record lists Belmont Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG?

The FDA product code for BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG is IWZ.

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Other records listing Belmont Equipment Corp. 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.

K000799BELMONT UNIT, MODEL 2000 SERIESK983661BELMONT UNIT, MODEL 6000 SERIES AND 7500 SERIESK963699BELRAY/MODEL 096, DENTAL INTRAORAL X-RAYK900681PANORAMIC MODEL X-CALIBER X-RAYK874238MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAYK870300BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75

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Related Devices (Code: IWZ)

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.

K970154KODAK EKTASIAN HG FILM (EHG-15)Eastman Kodak CompanyK954200VOXGRAMVoxelK9316043M MEDICAL DIAGNOSTIC VIDEOCASSETTE3M Health Care, Ltd.K9316053M MEDICAL DIAGNOSTIC SUPER VHS VIDEOCASSETTE3M Health Care, Ltd.K920539ORWO X-RAY FILMBurkhart Roentgen Intl., Inc.K884827KODAK DENTAL BARRIER PACEastman Kodak Company

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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