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FDA 510(k)

VIFS

K-Number: K955583 · 1996-05-14

ApplicantKonica Medical Corp.
Decision Date1996-05-14
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIFS is the device name listed in this FDA 510(k) record. The listed applicant is Konica Medical Corp.. It received FDA 510(k) clearance on 1996-05-14 under 510(k) number K955583. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIFS?

VIFS is a medical device that received FDA 510(k) clearance on 1996-05-14. The listed applicant is Konica Medical Corp.. The 510(k) number is K955583.

When did VIFS receive FDA 510(k) clearance?

VIFS received FDA 510(k) clearance on 1996-05-14, under 510(k) number K955583.

Who is the listed applicant for VIFS?

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

What is the FDA product code for VIFS?

The FDA product code for VIFS is JAK.

Other records listing Konica Medical 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.

K990969KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSORK963913MD100 & MM150K963914CM & CM DS-7K931316KONICA DS-7 AUTOMATIC X-RAY FILM PROCESSORK933830KONICA LD-4500 LASER DIGITIZERK931317KONICA SRX-301 AUTOMATIC X-RAY FILM PROCESSOR

View all 12 devices →

Related Devices (Code: JAK)

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.

K261125BodyTom 64 (NL4100); OmniTom Elite (NL5000)Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA View Phase 6.0Fujifilm CorporationK253836FCT iStream Phase 2Fujifilm CorporationK253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ SuiteGE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, LLC

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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