MOBILE CARRIER
K-Number: K781975 · 1978-12-04
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Device Summary
Frequently Asked Questions
What is the MOBILE CARRIER?
MOBILE CARRIER is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is General X-Ray, Inc.. The 510(k) number is K781975.
When did MOBILE CARRIER receive FDA 510(k) clearance?
MOBILE CARRIER received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781975.
Who is the listed applicant for MOBILE CARRIER?
The FDA 510(k) record lists General X-Ray, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOBILE CARRIER?
The FDA product code for MOBILE CARRIER is IZL.
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 General X-Ray, Inc. 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: IZL)
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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