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FDA 510(k)

FVP-1000 FAMILY AND FVP-1000D FAMILY

K-Number: K905694 · 1991-11-27

ApplicantFischer Imaging Corp.
Decision Date1991-11-27
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FVP-1000 FAMILY AND FVP-1000D FAMILY is the device name listed in this FDA 510(k) record. The listed applicant is Fischer Imaging Corp.. It received FDA 510(k) clearance on 1991-11-27 under 510(k) number K905694. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FVP-1000 FAMILY AND FVP-1000D FAMILY?

FVP-1000 FAMILY AND FVP-1000D FAMILY is a medical device that received FDA 510(k) clearance on 1991-11-27. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K905694.

When did FVP-1000 FAMILY AND FVP-1000D FAMILY receive FDA 510(k) clearance?

FVP-1000 FAMILY AND FVP-1000D FAMILY received FDA 510(k) clearance on 1991-11-27, under 510(k) number K905694.

Who is the listed applicant for FVP-1000 FAMILY AND FVP-1000D FAMILY?

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

What is the FDA product code for FVP-1000 FAMILY AND FVP-1000D FAMILY?

The FDA product code for FVP-1000 FAMILY AND FVP-1000D FAMILY is JAA.

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Other records listing Fischer Imaging Corp. as applicant

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K042095MAMMOTESTK021113MAMMOPATHK981414LC POSITIONERK973400MAMMOTEST ADAPTER DRIVERK964806MD-1835K961207EP-X BIPLANE

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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