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FDA 510(k)

SUNFLOWER

K-Number: K820123 · 1982-03-01

ApplicantSolana, Inc.
Decision Date1982-03-01
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUNFLOWER is the device name listed in this FDA 510(k) record. The listed applicant is Solana, Inc.. It received FDA 510(k) clearance on 1982-03-01 under 510(k) number K820123. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNFLOWER?

SUNFLOWER is a medical device that received FDA 510(k) clearance on 1982-03-01. The listed applicant is Solana, Inc.. The 510(k) number is K820123.

When did SUNFLOWER receive FDA 510(k) clearance?

SUNFLOWER received FDA 510(k) clearance on 1982-03-01, under 510(k) number K820123.

Who is the listed applicant for SUNFLOWER?

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

What is the FDA product code for SUNFLOWER?

The FDA product code for SUNFLOWER is FTC.

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Official Source

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