BASICAM COUNTER BALANCE CAMERA
K-Number: K850463 · 1985-04-10
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Device Summary
Frequently Asked Questions
What is the BASICAM COUNTER BALANCE CAMERA?
BASICAM COUNTER BALANCE CAMERA is a medical device that received FDA 510(k) clearance on 1985-04-10. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K850463.
When did BASICAM COUNTER BALANCE CAMERA receive FDA 510(k) clearance?
BASICAM COUNTER BALANCE CAMERA received FDA 510(k) clearance on 1985-04-10, under 510(k) number K850463.
Who is the listed applicant for BASICAM COUNTER BALANCE CAMERA?
The FDA 510(k) record lists Siemens Gammasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BASICAM COUNTER BALANCE CAMERA?
The FDA product code for BASICAM COUNTER BALANCE CAMERA is IYX.
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 Siemens Gammasonics, 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: IYX)
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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