CONDOMS (RAMSES, SHEIK AND KOROMEX)
K-Number: K882893 · 1988-10-26
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Device Summary
Frequently Asked Questions
What is the CONDOMS (RAMSES, SHEIK AND KOROMEX)?
CONDOMS (RAMSES, SHEIK AND KOROMEX) is a medical device that received FDA 510(k) clearance on 1988-10-26. The listed applicant is Schmid Laboratories, Inc.. The 510(k) number is K882893.
When did CONDOMS (RAMSES, SHEIK AND KOROMEX) receive FDA 510(k) clearance?
CONDOMS (RAMSES, SHEIK AND KOROMEX) received FDA 510(k) clearance on 1988-10-26, under 510(k) number K882893.
Who is the listed applicant for CONDOMS (RAMSES, SHEIK AND KOROMEX)?
The FDA 510(k) record lists Schmid Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONDOMS (RAMSES, SHEIK AND KOROMEX)?
The FDA product code for CONDOMS (RAMSES, SHEIK AND KOROMEX) 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 Schmid Laboratories, 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: 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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