OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C
K-Number: K993283 · 1999-12-29
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Device Summary
Frequently Asked Questions
What is the OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C?
OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C is a medical device that received FDA 510(k) clearance on 1999-12-29. The listed applicant is Arnold & Richter Cine Technik. The 510(k) number is K993283.
When did OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C receive FDA 510(k) clearance?
OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C received FDA 510(k) clearance on 1999-12-29, under 510(k) number K993283.
Who is the listed applicant for OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C?
The FDA 510(k) record lists Arnold & Richter Cine Technik as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C?
The FDA product code for OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C is LLZ.
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 Arnold & Richter Cine Technik 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: LLZ)
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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