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FDA 510(k)

VIEW MD OFFICE SYSTEM, MODEL 41066.5540

K-Number: K071292 · 2007-07-19

Decision Date2007-07-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VIEW MD OFFICE SYSTEM, MODEL 41066.5540 is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 2007-07-19 under 510(k) number K071292. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIEW MD OFFICE SYSTEM, MODEL 41066.5540?

VIEW MD OFFICE SYSTEM, MODEL 41066.5540 is a medical device that received FDA 510(k) clearance on 2007-07-19. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K071292.

When did VIEW MD OFFICE SYSTEM, MODEL 41066.5540 receive FDA 510(k) clearance?

VIEW MD OFFICE SYSTEM, MODEL 41066.5540 received FDA 510(k) clearance on 2007-07-19, under 510(k) number K071292.

Who is the listed applicant for VIEW MD OFFICE SYSTEM, MODEL 41066.5540?

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

What is the FDA product code for VIEW MD OFFICE SYSTEM, MODEL 41066.5540?

The FDA product code for VIEW MD OFFICE SYSTEM, MODEL 41066.5540 is GCJ.

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.

Other records listing Richard Wolf Medical Instruments 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.

View all 142 devices →

Related Devices (Code: GCJ)

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.

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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