LUBRICANT, OTRHO PERSONAL
K-Number: K790087 · 1979-02-01
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Device Summary
Frequently Asked Questions
What is the LUBRICANT, OTRHO PERSONAL?
LUBRICANT, OTRHO PERSONAL is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Ortho Pharmaceutical Corp.. The 510(k) number is K790087.
When did LUBRICANT, OTRHO PERSONAL receive FDA 510(k) clearance?
LUBRICANT, OTRHO PERSONAL received FDA 510(k) clearance on 1979-02-01, under 510(k) number K790087.
Who is the listed applicant for LUBRICANT, OTRHO PERSONAL?
The FDA 510(k) record lists Ortho Pharmaceutical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUBRICANT, OTRHO PERSONAL?
The FDA product code for LUBRICANT, OTRHO PERSONAL is KMJ.
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 Ortho Pharmaceutical Corp. 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: KMJ)
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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