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)

TOP DISPOSABLE INFUSION SET

K-Number: K841025 · 1984-03-30

Decision Date1984-03-30
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TOP DISPOSABLE INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Top Surgical Manufacturers Co.. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K841025. 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 TOP DISPOSABLE INFUSION SET?

TOP DISPOSABLE INFUSION SET is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Top Surgical Manufacturers Co.. The 510(k) number is K841025.

When did TOP DISPOSABLE INFUSION SET receive FDA 510(k) clearance?

TOP DISPOSABLE INFUSION SET received FDA 510(k) clearance on 1984-03-30, under 510(k) number K841025.

Who is the listed applicant for TOP DISPOSABLE INFUSION SET?

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

What is the FDA product code for TOP DISPOSABLE INFUSION SET?

The FDA product code for TOP DISPOSABLE INFUSION SET 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 Top Surgical Manufacturers 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 12 devices →

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.

↑