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FDA 510(k)

PROPHYLACTIC W/SPERMICIDAL LUBRICANT

K-Number: K802354 · 1980-09-25

ApplicantSchmid Laboratories, Inc.
Decision Date1980-09-25
Product Code
DecisionUnknown

Device Summary

PROPHYLACTIC W/SPERMICIDAL LUBRICANT 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 1980-09-25 under 510(k) number K802354. FDA Decision: Unknown.

Frequently Asked Questions

What is the PROPHYLACTIC W/SPERMICIDAL LUBRICANT?

PROPHYLACTIC W/SPERMICIDAL LUBRICANT is a medical device that received FDA 510(k) clearance on 1980-09-25. The listed applicant is Schmid Laboratories, Inc.. The 510(k) number is K802354.

When did PROPHYLACTIC W/SPERMICIDAL LUBRICANT receive FDA 510(k) clearance?

PROPHYLACTIC W/SPERMICIDAL LUBRICANT received FDA 510(k) clearance on 1980-09-25, under 510(k) number K802354.

Who is the listed applicant for PROPHYLACTIC W/SPERMICIDAL LUBRICANT?

The FDA 510(k) record lists Schmid Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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.

K897140THIN CONDOM RAMSES & SHEIKK900679MINT SCENTED CONDOMSK884399STANDARD LATEX CONDOMK882893CONDOMS (RAMSES, SHEIK AND KOROMEX)K880820OKAMOTO CONDOMS SPERMICIDALLY LUBRICATEDK874791CONDOMS (RAMSES EXTRA, SHEIK ELITE AND KOROMEX)

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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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