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FDA 510(k)

SATOBAN FIRST AID TAPE

K-Number: K823076 · 1983-01-12

Decision Date1983-01-12
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SATOBAN FIRST AID TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Food and Drug Service, Inc.. It received FDA 510(k) clearance on 1983-01-12 under 510(k) number K823076. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SATOBAN FIRST AID TAPE?

SATOBAN FIRST AID TAPE is a medical device that received FDA 510(k) clearance on 1983-01-12. The listed applicant is Food and Drug Service, Inc.. The 510(k) number is K823076.

When did SATOBAN FIRST AID TAPE receive FDA 510(k) clearance?

SATOBAN FIRST AID TAPE received FDA 510(k) clearance on 1983-01-12, under 510(k) number K823076.

Who is the listed applicant for SATOBAN FIRST AID TAPE?

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

What is the FDA product code for SATOBAN FIRST AID TAPE?

The FDA product code for SATOBAN FIRST AID TAPE is KGX.

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 Food and Drug Service, 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: KGX)

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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