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FDA 510(k)

VISCO HANDEX-VARIOUS MODELS

K-Number: K821855 · 1982-07-02

ApplicantFred Sammons, Inc.
Decision Date1982-07-02
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VISCO HANDEX-VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1982-07-02 under 510(k) number K821855. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISCO HANDEX-VARIOUS MODELS?

VISCO HANDEX-VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K821855.

When did VISCO HANDEX-VARIOUS MODELS receive FDA 510(k) clearance?

VISCO HANDEX-VARIOUS MODELS received FDA 510(k) clearance on 1982-07-02, under 510(k) number K821855.

Who is the listed applicant for VISCO HANDEX-VARIOUS MODELS?

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

What is the FDA product code for VISCO HANDEX-VARIOUS MODELS?

The FDA product code for VISCO HANDEX-VARIOUS MODELS is ION.

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Related Devices (Code: ION)

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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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