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FDA 510(k)

VISUALAX

K-Number: K781634 · 1978-10-03

ApplicantFarrall Instruments, Inc.
Decision Date1978-10-03
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VISUALAX is the device name listed in this FDA 510(k) record. The listed applicant is Farrall Instruments, Inc.. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K781634. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISUALAX?

VISUALAX is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Farrall Instruments, Inc.. The 510(k) number is K781634.

When did VISUALAX receive FDA 510(k) clearance?

VISUALAX received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781634.

Who is the listed applicant for VISUALAX?

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

What is the FDA product code for VISUALAX?

The FDA product code for VISUALAX is HCC.

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Other records listing Farrall Instruments, Inc. as applicant

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K940128CAT-400UL PENILE PLETHYSMOGRAPHK936115CAT-600 PENILE PLETHYSMOGRAPHK821723BI-4520 DUAL IMPEDOMETERK821664PP-100, PERSONAL PERINEOMETERK792305A SLEEP ASSESSMENT DEVICEK760166STIMULATOR, SONIC CONTROL (AS-1)

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Related Devices (Code: HCC)

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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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