CANON X-RAY I.I. RAPID SEQUENCE CAMERA CRS-105
K-Number: K853861 · 1985-10-24
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Device Summary
Frequently Asked Questions
What is the CANON X-RAY I.I. RAPID SEQUENCE CAMERA CRS-105?
CANON X-RAY I.I. RAPID SEQUENCE CAMERA CRS-105 is a medical device that received FDA 510(k) clearance on 1985-10-24. The listed applicant is Canon USA, Inc.. The 510(k) number is K853861.
When did CANON X-RAY I.I. RAPID SEQUENCE CAMERA CRS-105 receive FDA 510(k) clearance?
CANON X-RAY I.I. RAPID SEQUENCE CAMERA CRS-105 received FDA 510(k) clearance on 1985-10-24, under 510(k) number K853861.
Who is the listed applicant for CANON X-RAY I.I. RAPID SEQUENCE CAMERA CRS-105?
The FDA 510(k) record lists Canon USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CANON X-RAY I.I. RAPID SEQUENCE CAMERA CRS-105?
The FDA product code for CANON X-RAY I.I. RAPID SEQUENCE CAMERA CRS-105 is IJZ.
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 Canon USA, 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.
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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