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FDA 510(k)

SCAN BAND

K-Number: K923106 · 1992-09-11

ApplicantCook, Inc.
Decision Date1992-09-11
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SCAN BAND is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1992-09-11 under 510(k) number K923106. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCAN BAND?

SCAN BAND is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Cook, Inc.. The 510(k) number is K923106.

When did SCAN BAND receive FDA 510(k) clearance?

SCAN BAND received FDA 510(k) clearance on 1992-09-11, under 510(k) number K923106.

Who is the listed applicant for SCAN BAND?

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

What is the FDA product code for SCAN BAND?

The FDA product code for SCAN BAND is JAK.

Other records listing Cook, 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.

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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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