TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL
K-Number: K912696 · 1991-09-16
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Device Summary
Frequently Asked Questions
What is the TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL?
TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL is a medical device that received FDA 510(k) clearance on 1991-09-16. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K912696.
When did TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL receive FDA 510(k) clearance?
TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL received FDA 510(k) clearance on 1991-09-16, under 510(k) number K912696.
Who is the listed applicant for TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL?
The FDA 510(k) record lists Bennett X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL?
The FDA product code for TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL is IYB.
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 Bennett X-Ray 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: IYB)
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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