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FDA 510(k)

HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION

K-Number: K002782 · 2000-12-05

ApplicantNuclear Diagnostics AB
Decision Date2000-12-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Diagnostics AB. It received FDA 510(k) clearance on 2000-12-05 under 510(k) number K002782. 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 HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION?

HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION is a medical device that received FDA 510(k) clearance on 2000-12-05. The listed applicant is Nuclear Diagnostics AB. The 510(k) number is K002782.

When did HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION receive FDA 510(k) clearance?

HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION received FDA 510(k) clearance on 2000-12-05, under 510(k) number K002782.

Who is the listed applicant for HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION?

The FDA 510(k) record lists Nuclear Diagnostics AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION?

The FDA product code for HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION is 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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