LOVESAFE DOTTY CONDOM ONE DZ. CODOMS/BOX, DC-20
K-Number: K851292 · 1985-05-23
Advertisement
Device Summary
Frequently Asked Questions
What is the LOVESAFE DOTTY CONDOM ONE DZ. CODOMS/BOX, DC-20?
LOVESAFE DOTTY CONDOM ONE DZ. CODOMS/BOX, DC-20 is a medical device that received FDA 510(k) clearance on 1985-05-23. The listed applicant is Manexim Multicorp, Ltd.. The 510(k) number is K851292.
When did LOVESAFE DOTTY CONDOM ONE DZ. CODOMS/BOX, DC-20 receive FDA 510(k) clearance?
LOVESAFE DOTTY CONDOM ONE DZ. CODOMS/BOX, DC-20 received FDA 510(k) clearance on 1985-05-23, under 510(k) number K851292.
Who is the listed applicant for LOVESAFE DOTTY CONDOM ONE DZ. CODOMS/BOX, DC-20?
The FDA 510(k) record lists Manexim Multicorp, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOVESAFE DOTTY CONDOM ONE DZ. CODOMS/BOX, DC-20?
The FDA product code for LOVESAFE DOTTY CONDOM ONE DZ. CODOMS/BOX, DC-20 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 Manexim Multicorp, Ltd. 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.
Advertisement