INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION)
K-Number: K891176 · 1989-05-18
Advertisement
Device Summary
Frequently Asked Questions
What is the INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION)?
INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION) is a medical device that received FDA 510(k) clearance on 1989-05-18. The listed applicant is Multi-Med, Inc.. The 510(k) number is K891176.
When did INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION) receive FDA 510(k) clearance?
INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION) received FDA 510(k) clearance on 1989-05-18, under 510(k) number K891176.
Who is the listed applicant for INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION)?
The FDA 510(k) record lists Multi-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION)?
The FDA product code for INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION) 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 Multi-Med, Inc. 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.
Advertisement