A901 TILT IN SPACE
K-Number: K933853 · 1994-03-28
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Device Summary
Frequently Asked Questions
What is the A901 TILT IN SPACE?
A901 TILT IN SPACE 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 K933853.
When did A901 TILT IN SPACE receive FDA 510(k) clearance?
A901 TILT IN SPACE received FDA 510(k) clearance on 1994-03-28, under 510(k) number K933853.
Who is the listed applicant for A901 TILT IN SPACE?
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 A901 TILT IN SPACE?
The FDA product code for A901 TILT IN SPACE 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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