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FDA 510(k)

CHILI VIDEO, CHILI VIDEOPRO

K-Number: K000411 · 2000-04-14

Decision Date2000-04-14
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CHILI VIDEO, CHILI VIDEOPRO is the device name listed in this FDA 510(k) record. The listed applicant is Steinbeis-Transferzentrum Medizinische Informatik. It received FDA 510(k) clearance on 2000-04-14 under 510(k) number K000411. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHILI VIDEO, CHILI VIDEOPRO?

CHILI VIDEO, CHILI VIDEOPRO is a medical device that received FDA 510(k) clearance on 2000-04-14. The listed applicant is Steinbeis-Transferzentrum Medizinische Informatik. The 510(k) number is K000411.

When did CHILI VIDEO, CHILI VIDEOPRO receive FDA 510(k) clearance?

CHILI VIDEO, CHILI VIDEOPRO received FDA 510(k) clearance on 2000-04-14, under 510(k) number K000411.

Who is the listed applicant for CHILI VIDEO, CHILI VIDEOPRO?

The FDA 510(k) record lists Steinbeis-Transferzentrum Medizinische Informatik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHILI VIDEO, CHILI VIDEOPRO?

The FDA product code for CHILI VIDEO, CHILI VIDEOPRO is LMA.

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.

Related Devices (Code: LMA)

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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