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FDA 510(k)

SOLVALINE

K-Number: K802790 · 1981-02-13

ApplicantSecol Co.
Decision Date1981-02-13
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SOLVALINE is the device name listed in this FDA 510(k) record. The listed applicant is Secol Co.. It received FDA 510(k) clearance on 1981-02-13 under 510(k) number K802790. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLVALINE?

SOLVALINE is a medical device that received FDA 510(k) clearance on 1981-02-13. The listed applicant is Secol Co.. The 510(k) number is K802790.

When did SOLVALINE receive FDA 510(k) clearance?

SOLVALINE received FDA 510(k) clearance on 1981-02-13, under 510(k) number K802790.

Who is the listed applicant for SOLVALINE?

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

What is the FDA product code for SOLVALINE?

The FDA product code for SOLVALINE is KKX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Secol Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 18 devices →

Related Devices (Code: KKX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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