STANDARD LATEX CONDOMS (RAMSES, SHEIK AND KOROMEX)— 510(k) K874718

Name: FDA 510(k) clearance K874718
Creator: U.S. Food and Drug Administration
Published: 1987-12-08

Substantially Equivalent

Schmid Laboratories, Inc.

FDA 510(k) clearance K874718 for STANDARD LATEX CONDOMS (RAMSES, SHEIK AND KOROMEX), Substantially Equivalent on 1987-12-08. 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: 1987-11-17
Decision date: 1987-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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
K900679 — MINT SCENTED CONDOMS1990-06-07
K884399 — STANDARD LATEX CONDOM1989-03-01
K882893 — CONDOMS (RAMSES, SHEIK AND KOROMEX)1988-10-26
K880820 — OKAMOTO CONDOMS SPERMICIDALLY LUBRICATED1988-06-21

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