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)

SAFETY SUBCUTANEOUS TISSUE INFUSION SET

K-Number: K120195 · 2012-07-06

ApplicantMulti Med
Decision Date2012-07-06
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFETY SUBCUTANEOUS TISSUE INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Multi Med. It received FDA 510(k) clearance on 2012-07-06 under 510(k) number K120195. 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 SAFETY SUBCUTANEOUS TISSUE INFUSION SET?

SAFETY SUBCUTANEOUS TISSUE INFUSION SET is a medical device that received FDA 510(k) clearance on 2012-07-06. The listed applicant is Multi Med. The 510(k) number is K120195.

When did SAFETY SUBCUTANEOUS TISSUE INFUSION SET receive FDA 510(k) clearance?

SAFETY SUBCUTANEOUS TISSUE INFUSION SET received FDA 510(k) clearance on 2012-07-06, under 510(k) number K120195.

Who is the listed applicant for SAFETY SUBCUTANEOUS TISSUE INFUSION SET?

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

What is the FDA product code for SAFETY SUBCUTANEOUS TISSUE INFUSION SET?

The FDA product code for SAFETY SUBCUTANEOUS TISSUE 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.

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.

↑