MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325
K-Number: K023938 · 2002-12-13
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325?
MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325 is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Hutchinson Technology, Inc.. The 510(k) number is K023938.
When did MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325 receive FDA 510(k) clearance?
MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325 received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023938.
Who is the listed applicant for MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325?
The FDA 510(k) record lists Hutchinson Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325?
The FDA product code for MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325 is MUD.
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 Hutchinson Technology, Inc. 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: MUD)
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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