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FDA 510(k)

FRANTZ IMAGING COMPACT CAMERA

K-Number: K871959 · 1987-06-22

ApplicantFrantz Imaging, Inc.
Decision Date1987-06-22
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FRANTZ IMAGING COMPACT CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Frantz Imaging, Inc.. It received FDA 510(k) clearance on 1987-06-22 under 510(k) number K871959. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRANTZ IMAGING COMPACT CAMERA?

FRANTZ IMAGING COMPACT CAMERA is a medical device that received FDA 510(k) clearance on 1987-06-22. The listed applicant is Frantz Imaging, Inc.. The 510(k) number is K871959.

When did FRANTZ IMAGING COMPACT CAMERA receive FDA 510(k) clearance?

FRANTZ IMAGING COMPACT CAMERA received FDA 510(k) clearance on 1987-06-22, under 510(k) number K871959.

Who is the listed applicant for FRANTZ IMAGING COMPACT CAMERA?

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

What is the FDA product code for FRANTZ IMAGING COMPACT CAMERA?

The FDA product code for FRANTZ IMAGING COMPACT CAMERA is LMC.

Related Clinical Trials

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.

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Other records listing Frantz Imaging, 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.

K952485LASERNET IMAGE MANAGER/PRINT SERVERK921215LASERSTAR IMAGERK871957SPACEMISER 8-10 FILM RECORDERK871958SPACEMISER 8-17 FILM RECORDER

Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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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