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FDA 510(k)

CHANNEL BACK

K-Number: K823093 · 1982-11-16

ApplicantJ.G. Shuman Assoc.
Decision Date1982-11-16
Product Code
DecisionSubstantially Equivalent

Device Summary

CHANNEL BACK is the device name listed in this FDA 510(k) record. The listed applicant is J.G. Shuman Assoc.. It received FDA 510(k) clearance on 1982-11-16 under 510(k) number K823093. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHANNEL BACK?

CHANNEL BACK is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is J.G. Shuman Assoc.. The 510(k) number is K823093.

When did CHANNEL BACK receive FDA 510(k) clearance?

CHANNEL BACK received FDA 510(k) clearance on 1982-11-16, under 510(k) number K823093.

Who is the listed applicant for CHANNEL BACK?

The FDA 510(k) record lists J.G. Shuman Assoc. as the applicant. This does not by itself establish the device manufacturer.

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.

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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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