SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM
K-Number: K943933 · 1995-06-22
Advertisement
Device Summary
Frequently Asked Questions
What is the SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM?
SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is Aladan Corp.. The 510(k) number is K943933.
When did SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM receive FDA 510(k) clearance?
SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM received FDA 510(k) clearance on 1995-06-22, under 510(k) number K943933.
Who is the listed applicant for SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM?
The FDA 510(k) record lists Aladan Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM?
The FDA product code for SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM 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 Aladan Corp. 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