Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SOLUTION ADMIN. SET STERILE

K-Number: K840410 · 1984-03-19

ApplicantLoversan
Decision Date1984-03-19
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SOLUTION ADMIN. SET STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Loversan. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K840410. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLUTION ADMIN. SET STERILE?

SOLUTION ADMIN. SET STERILE is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Loversan. The 510(k) number is K840410.

When did SOLUTION ADMIN. SET STERILE receive FDA 510(k) clearance?

SOLUTION ADMIN. SET STERILE received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840410.

Who is the listed applicant for SOLUTION ADMIN. SET STERILE?

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

What is the FDA product code for SOLUTION ADMIN. SET STERILE?

The FDA product code for SOLUTION ADMIN. SET STERILE is FPA.

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 Loversan 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.

Related Devices (Code: FPA)

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.

↑