PAMITEX,LONG LOVE,DESIRE,SKIN LESS,GINZA,LOVE TIME
K-Number: K864570 · 1986-12-30
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Device Summary
Frequently Asked Questions
What is the PAMITEX,LONG LOVE,DESIRE,SKIN LESS,GINZA,LOVE TIME?
PAMITEX,LONG LOVE,DESIRE,SKIN LESS,GINZA,LOVE TIME is a medical device that received FDA 510(k) clearance on 1986-12-30. The listed applicant is Dongkuk Techco Rubber Industries. The 510(k) number is K864570.
When did PAMITEX,LONG LOVE,DESIRE,SKIN LESS,GINZA,LOVE TIME receive FDA 510(k) clearance?
PAMITEX,LONG LOVE,DESIRE,SKIN LESS,GINZA,LOVE TIME received FDA 510(k) clearance on 1986-12-30, under 510(k) number K864570.
Who is the listed applicant for PAMITEX,LONG LOVE,DESIRE,SKIN LESS,GINZA,LOVE TIME?
The FDA 510(k) record lists Dongkuk Techco Rubber Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PAMITEX,LONG LOVE,DESIRE,SKIN LESS,GINZA,LOVE TIME?
The FDA product code for PAMITEX,LONG LOVE,DESIRE,SKIN LESS,GINZA,LOVE TIME is HIS.
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 Dongkuk Techco Rubber Industries 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: HIS)
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
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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