FDA 510(k)

TENDERM TAPE

K-Number: K863194 · 1986-09-30

Decision Date1986-09-30

Product Code

DecisionSubstantially Equivalent

Device Summary

TENDERM TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Lectec Corp.. It received FDA 510(k) clearance on 1986-09-30 under 510(k) number K863194. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENDERM TAPE?

TENDERM TAPE is a medical device that received FDA 510(k) clearance on 1986-09-30. The listed applicant is Lectec Corp.. The 510(k) number is K863194.

When did TENDERM TAPE receive FDA 510(k) clearance?

TENDERM TAPE received FDA 510(k) clearance on 1986-09-30, under 510(k) number K863194.

Who is the listed applicant for TENDERM TAPE?

The FDA 510(k) record lists Lectec Corp. 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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Other records listing Lectec Corp. as applicant

K950943ULTRA EASE K925384ISOPORE(TM) TAPE, MODIFICATION K930258TRACET T-6000 K923558ECG ELECTRODE K922959ISOPORE TAPE K912450TRACETS SME 5000

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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.