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FDA 510(k)

PHOTOPHONE

K-Number: K896223 · 1990-02-12

ApplicantImage Data Corp.
Decision Date1990-02-12
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHOTOPHONE is the device name listed in this FDA 510(k) record. The listed applicant is Image Data Corp.. It received FDA 510(k) clearance on 1990-02-12 under 510(k) number K896223. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTOPHONE?

PHOTOPHONE is a medical device that received FDA 510(k) clearance on 1990-02-12. The listed applicant is Image Data Corp.. The 510(k) number is K896223.

When did PHOTOPHONE receive FDA 510(k) clearance?

PHOTOPHONE received FDA 510(k) clearance on 1990-02-12, under 510(k) number K896223.

Who is the listed applicant for PHOTOPHONE?

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

What is the FDA product code for PHOTOPHONE?

The FDA product code for PHOTOPHONE is LMA.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Image Data 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.

K931186PHOTOPHONE MULTIVIEWK931292MULTIVIEW FOR WINDOWSK931060STATVIEWK922267PHOTOPHONE(R) MULTI VIEW(TM)K921527STATVIEW

Related Devices (Code: LMA)

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.

K132183DICOM VIDEOBar Code Computer, Ltd.K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDVidar Systems Corp.K130406DIAGNOSTICPRO EDGEVidar Systems Corp.K102476TELERADPROVidar Systems Corp.K093809VIDAR DENTAL FILM DIGITIZERVidar Systems Corp.K091288MEDI-6000 MEDICAL IMAGE DIGITIZERMicrotek International, 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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