GILB, MODEL 8010
K-Number: K011200 · 2001-06-14
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Device Summary
Frequently Asked Questions
What is the GILB, MODEL 8010?
GILB, MODEL 8010 is a medical device that received FDA 510(k) clearance on 2001-06-14. The listed applicant is 3M Company. The 510(k) number is K011200.
When did GILB, MODEL 8010 receive FDA 510(k) clearance?
GILB, MODEL 8010 received FDA 510(k) clearance on 2001-06-14, under 510(k) number K011200.
Who is the listed applicant for GILB, MODEL 8010?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GILB, MODEL 8010?
The FDA product code for GILB, MODEL 8010 is EMA.
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 3M Company 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: EMA)
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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