RADIAL TRAVEL SPEC. PROCEDURES TABLE
K-Number: K761339 · 1977-01-05
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Device Summary
Frequently Asked Questions
What is the RADIAL TRAVEL SPEC. PROCEDURES TABLE?
RADIAL TRAVEL SPEC. PROCEDURES TABLE is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Xre Corp.. The 510(k) number is K761339.
When did RADIAL TRAVEL SPEC. PROCEDURES TABLE receive FDA 510(k) clearance?
RADIAL TRAVEL SPEC. PROCEDURES TABLE received FDA 510(k) clearance on 1977-01-05, under 510(k) number K761339.
Who is the listed applicant for RADIAL TRAVEL SPEC. PROCEDURES TABLE?
The FDA 510(k) record lists Xre Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RADIAL TRAVEL SPEC. PROCEDURES TABLE?
The FDA product code for RADIAL TRAVEL SPEC. PROCEDURES TABLE is IZZ.
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 Xre 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: IZZ)
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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