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FDA 510(k)

MINT SCENTED CONDOMS

K-Number: K900679 · 1990-06-07

Decision Date1990-06-07
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINT SCENTED CONDOMS is the device name listed in this FDA 510(k) record. The listed applicant is Schmid Laboratories, Inc.. It received FDA 510(k) clearance on 1990-06-07 under 510(k) number K900679. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINT SCENTED CONDOMS?

MINT SCENTED CONDOMS is a medical device that received FDA 510(k) clearance on 1990-06-07. The listed applicant is Schmid Laboratories, Inc.. The 510(k) number is K900679.

When did MINT SCENTED CONDOMS receive FDA 510(k) clearance?

MINT SCENTED CONDOMS received FDA 510(k) clearance on 1990-06-07, under 510(k) number K900679.

Who is the listed applicant for MINT SCENTED CONDOMS?

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 MINT SCENTED CONDOMS?

The FDA product code for MINT SCENTED CONDOMS 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.

View all 10 devices →

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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