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)

PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606

K-Number: K041919 · 2004-10-04

ApplicantClinico
Decision Date2004-10-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606 is the device name listed in this FDA 510(k) record. The listed applicant is Clinico. It received FDA 510(k) clearance on 2004-10-04 under 510(k) number K041919. 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 PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606?

PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606 is a medical device that received FDA 510(k) clearance on 2004-10-04. The listed applicant is Clinico. The 510(k) number is K041919.

When did PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606 receive FDA 510(k) clearance?

PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606 received FDA 510(k) clearance on 2004-10-04, under 510(k) number K041919.

Who is the listed applicant for PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606?

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

What is the FDA product code for PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606?

The FDA product code for PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606 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 Clinico 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.

↑