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)

ADMINISTRATION SETS WITH BALL FLOAT

K-Number: K951922 · 1995-07-19

ApplicantImed Corp.
Decision Date1995-07-19
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADMINISTRATION SETS WITH BALL FLOAT is the device name listed in this FDA 510(k) record. The listed applicant is Imed Corp.. It received FDA 510(k) clearance on 1995-07-19 under 510(k) number K951922. 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 ADMINISTRATION SETS WITH BALL FLOAT?

ADMINISTRATION SETS WITH BALL FLOAT is a medical device that received FDA 510(k) clearance on 1995-07-19. The listed applicant is Imed Corp.. The 510(k) number is K951922.

When did ADMINISTRATION SETS WITH BALL FLOAT receive FDA 510(k) clearance?

ADMINISTRATION SETS WITH BALL FLOAT received FDA 510(k) clearance on 1995-07-19, under 510(k) number K951922.

Who is the listed applicant for ADMINISTRATION SETS WITH BALL FLOAT?

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

What is the FDA product code for ADMINISTRATION SETS WITH BALL FLOAT?

The FDA product code for ADMINISTRATION SETS WITH BALL FLOAT 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 Imed Corp. 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 43 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.

↑