AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING
K-Number: K130345 · 2013-08-01
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Device Summary
Frequently Asked Questions
What is the AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING?
AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING is a medical device that received FDA 510(k) clearance on 2013-08-01. The listed applicant is Mayer Laboratories, Inc.. The 510(k) number is K130345.
When did AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING receive FDA 510(k) clearance?
AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING received FDA 510(k) clearance on 2013-08-01, under 510(k) number K130345.
Who is the listed applicant for AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING?
The FDA 510(k) record lists Mayer Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING?
The FDA product code for AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING is NUC.
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 Mayer 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.
Related Devices (Code: NUC)
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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