GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES
K-Number: K941973 · 1995-06-30
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Device Summary
Frequently Asked Questions
What is the GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES?
GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES is a medical device that received FDA 510(k) clearance on 1995-06-30. The listed applicant is Medi-Globe Corp.. The 510(k) number is K941973.
When did GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES receive FDA 510(k) clearance?
GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES received FDA 510(k) clearance on 1995-06-30, under 510(k) number K941973.
Who is the listed applicant for GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES?
The FDA 510(k) record lists Medi-Globe Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES?
The FDA product code for GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES is FGE.
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 Medi-Globe 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.
Related Devices (Code: FGE)
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.
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