Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C

K-Number: K993283 · 1999-12-29

Decision Date1999-12-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C is the device name listed in this FDA 510(k) record. The listed applicant is Arnold & Richter Cine Technik. It received FDA 510(k) clearance on 1999-12-29 under 510(k) number K993283. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

↑