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FDA 510(k)

ENDOSCOPIC LIGHT SOURCE

K-Number: K885183 · 1989-03-09

Decision Date1989-03-09
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Technology For Imaging, Inc.. It received FDA 510(k) clearance on 1989-03-09 under 510(k) number K885183. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC LIGHT SOURCE?

ENDOSCOPIC LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1989-03-09. The listed applicant is Technology For Imaging, Inc.. The 510(k) number is K885183.

When did ENDOSCOPIC LIGHT SOURCE receive FDA 510(k) clearance?

ENDOSCOPIC LIGHT SOURCE received FDA 510(k) clearance on 1989-03-09, under 510(k) number K885183.

Who is the listed applicant for ENDOSCOPIC LIGHT SOURCE?

The FDA 510(k) record lists Technology For Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPIC LIGHT SOURCE?

The FDA product code for ENDOSCOPIC LIGHT SOURCE is HRX.

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 Technology For Imaging, 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: HRX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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