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FDA 510(k)

FOTOMASTER

K-Number: K000380 · 2000-05-03

ApplicantHamilton Thorne Research
Decision Date2000-05-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FOTOMASTER is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Thorne Research. It received FDA 510(k) clearance on 2000-05-03 under 510(k) number K000380. 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 FOTOMASTER?

FOTOMASTER is a medical device that received FDA 510(k) clearance on 2000-05-03. The listed applicant is Hamilton Thorne Research. The 510(k) number is K000380.

When did FOTOMASTER receive FDA 510(k) clearance?

FOTOMASTER received FDA 510(k) clearance on 2000-05-03, under 510(k) number K000380.

Who is the listed applicant for FOTOMASTER?

The FDA 510(k) record lists Hamilton Thorne Research as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FOTOMASTER?

The FDA product code for FOTOMASTER is LLZ.

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Other records listing Hamilton Thorne Research 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.

K012805AUTOMARQERK990184AUTOMARQERK920719IVOS ANALYZERK873172HAMILTON-THORN MOTILITY ANALYZER HTM-2000

Related Devices (Code: LLZ)

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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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