REGULAR MAXITHINS PADS & SUPER MAXITHINS
K-Number: K821800 · 1982-06-25
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Device Summary
Frequently Asked Questions
What is the REGULAR MAXITHINS PADS & SUPER MAXITHINS?
REGULAR MAXITHINS PADS & SUPER MAXITHINS is a medical device that received FDA 510(k) clearance on 1982-06-25. The listed applicant is Tampax, Inc.. The 510(k) number is K821800.
When did REGULAR MAXITHINS PADS & SUPER MAXITHINS receive FDA 510(k) clearance?
REGULAR MAXITHINS PADS & SUPER MAXITHINS received FDA 510(k) clearance on 1982-06-25, under 510(k) number K821800.
Who is the listed applicant for REGULAR MAXITHINS PADS & SUPER MAXITHINS?
The FDA 510(k) record lists Tampax, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REGULAR MAXITHINS PADS & SUPER MAXITHINS?
The FDA product code for REGULAR MAXITHINS PADS & SUPER MAXITHINS is HHD.
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 Tampax, 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: HHD)
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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