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FDA 510(k)

INNOSCAN EXAMINATION LIGHT

K-Number: K827796 · 1982-08-24

ApplicantInnomed Corp.
Decision Date1982-08-24
Product Code
DecisionSubstantially Equivalent

Device Summary

INNOSCAN EXAMINATION LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Innomed Corp.. It received FDA 510(k) clearance on 1982-08-24 under 510(k) number K827796. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INNOSCAN EXAMINATION LIGHT?

INNOSCAN EXAMINATION LIGHT is a medical device that received FDA 510(k) clearance on 1982-08-24. The listed applicant is Innomed Corp.. The 510(k) number is K827796.

When did INNOSCAN EXAMINATION LIGHT receive FDA 510(k) clearance?

INNOSCAN EXAMINATION LIGHT received FDA 510(k) clearance on 1982-08-24, under 510(k) number K827796.

Who is the listed applicant for INNOSCAN EXAMINATION LIGHT?

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

Related Clinical Trials

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Other records listing Innomed Corp. 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.

K872747LASER CENTERING DEVICEK822574INNOMED PD-1 KIT

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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