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FDA 510(k)

LVV OPTION

K-Number: K781855 · 1979-01-05

ApplicantHoneywell, Inc.
Decision Date1979-01-05
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LVV OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1979-01-05 under 510(k) number K781855. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LVV OPTION?

LVV OPTION is a medical device that received FDA 510(k) clearance on 1979-01-05. The listed applicant is Honeywell, Inc.. The 510(k) number is K781855.

When did LVV OPTION receive FDA 510(k) clearance?

LVV OPTION received FDA 510(k) clearance on 1979-01-05, under 510(k) number K781855.

Who is the listed applicant for LVV OPTION?

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

What is the FDA product code for LVV OPTION?

The FDA product code for LVV OPTION is DXG.

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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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