MAXI PADS SCENTED DEODORIZED
K-Number: K831693 · 1983-06-16
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Device Summary
Frequently Asked Questions
What is the MAXI PADS SCENTED DEODORIZED?
MAXI PADS SCENTED DEODORIZED is a medical device that received FDA 510(k) clearance on 1983-06-16. The listed applicant is Int'L Consumer Disposables. The 510(k) number is K831693.
When did MAXI PADS SCENTED DEODORIZED receive FDA 510(k) clearance?
MAXI PADS SCENTED DEODORIZED received FDA 510(k) clearance on 1983-06-16, under 510(k) number K831693.
Who is the listed applicant for MAXI PADS SCENTED DEODORIZED?
The FDA 510(k) record lists Int'L Consumer Disposables as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXI PADS SCENTED DEODORIZED?
The FDA product code for MAXI PADS SCENTED DEODORIZED is HHL.
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 Int'L Consumer Disposables 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: HHL)
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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