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FDA 510(k)

ADHESIVE TRACTION TAPE

K-Number: K834142 · 1984-04-23

Decision Date1984-04-23
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADHESIVE TRACTION TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1984-04-23 under 510(k) number K834142. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADHESIVE TRACTION TAPE?

ADHESIVE TRACTION TAPE is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Devon Industries, Inc.. The 510(k) number is K834142.

When did ADHESIVE TRACTION TAPE receive FDA 510(k) clearance?

ADHESIVE TRACTION TAPE received FDA 510(k) clearance on 1984-04-23, under 510(k) number K834142.

Who is the listed applicant for ADHESIVE TRACTION TAPE?

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

What is the FDA product code for ADHESIVE TRACTION TAPE?

The FDA product code for ADHESIVE TRACTION TAPE is GAD.

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 Devon Industries, 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.

View all 47 devices →

Related Devices (Code: GAD)

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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