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FDA 510(k)

MODEL IV 6500 FORMULATOR

K-Number: K792142 · 1979-11-29

ApplicantValleylab, Inc.
Decision Date1979-11-29
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL IV 6500 FORMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1979-11-29 under 510(k) number K792142. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL IV 6500 FORMULATOR?

MODEL IV 6500 FORMULATOR is a medical device that received FDA 510(k) clearance on 1979-11-29. The listed applicant is Valleylab, Inc.. The 510(k) number is K792142.

When did MODEL IV 6500 FORMULATOR receive FDA 510(k) clearance?

MODEL IV 6500 FORMULATOR received FDA 510(k) clearance on 1979-11-29, under 510(k) number K792142.

Who is the listed applicant for MODEL IV 6500 FORMULATOR?

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

What is the FDA product code for MODEL IV 6500 FORMULATOR?

The FDA product code for MODEL IV 6500 FORMULATOR is FRN.

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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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