770 POWER BASE
K-Number: K933854 · 1994-03-28
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Device Summary
Frequently Asked Questions
What is the 770 POWER BASE?
770 POWER BASE is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Fortress Scientific , Ltd.. The 510(k) number is K933854.
When did 770 POWER BASE receive FDA 510(k) clearance?
770 POWER BASE received FDA 510(k) clearance on 1994-03-28, under 510(k) number K933854.
Who is the listed applicant for 770 POWER BASE?
The FDA 510(k) record lists Fortress Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 770 POWER BASE?
The FDA product code for 770 POWER BASE is ITI.
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 Fortress Scientific , Ltd. 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: ITI)
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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