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FDA 510(k)

MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER

K-Number: K844132 · 1985-01-22

ApplicantSigma Teleproducts, Inc.
Decision Date1985-01-22
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Teleproducts, Inc.. It received FDA 510(k) clearance on 1985-01-22 under 510(k) number K844132. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER?

MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER is a medical device that received FDA 510(k) clearance on 1985-01-22. The listed applicant is Sigma Teleproducts, Inc.. The 510(k) number is K844132.

When did MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER receive FDA 510(k) clearance?

MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER received FDA 510(k) clearance on 1985-01-22, under 510(k) number K844132.

Who is the listed applicant for MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER?

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

What is the FDA product code for MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER?

The FDA product code for MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER is LMB.

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Related Devices (Code: LMB)

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.

K992131SAMSUNG RAYPAX LONG TERM ARCHIVESamsung Sds Co., Ltd.K984405ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000Intracom Corp.K983447WISE (II) IMAGE MANAGEMENT SYSTEMSectra-Imtec ABK980243PARAMETER DEVELOPMENTS DICOM ARCHIVAL SERVER, (DAS)/DICOM INTRANET SERVICE (DIS)Parameter Developments, Inc.K973463OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVEO Tech, Inc.K973413ID. STORE (RELEASE 2.0)I.S.G. Technologies, 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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