CONDOMS (RAMSES, SHEIK AND KOROMEX)— 510(k) K882893

Name: FDA 510(k) clearance K882893
Creator: U.S. Food and Drug Administration
Published: 1988-10-26

Substantially Equivalent

Schmid Laboratories, Inc.

FDA 510(k) clearance K882893 for CONDOMS (RAMSES, SHEIK AND KOROMEX), Substantially Equivalent on 1988-10-26. Applicant: Schmid Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Schmid Laboratories, Inc.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1988-07-11
Decision date: 1988-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Little Falls, NJ, US

Download summary PDF View on FDA.gov ↗

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More clearances from Schmid Laboratories, Inc.

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K897140 — THIN CONDOM RAMSES & SHEIK1990-07-13
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K874791 — CONDOMS (RAMSES EXTRA, SHEIK ELITE AND KOROMEX)1988-04-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.