MALE INSERT SLIP
K-Number: K840482 · 1984-02-21
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Device Summary
Frequently Asked Questions
What is the MALE INSERT SLIP?
MALE INSERT SLIP is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Beghin_Say Intl., Inc.. The 510(k) number is K840482.
When did MALE INSERT SLIP receive FDA 510(k) clearance?
MALE INSERT SLIP received FDA 510(k) clearance on 1984-02-21, under 510(k) number K840482.
Who is the listed applicant for MALE INSERT SLIP?
The FDA 510(k) record lists Beghin_Say Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MALE INSERT SLIP?
The FDA product code for MALE INSERT SLIP is EYQ.
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 Beghin_Say Intl., 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: EYQ)
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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