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FDA 510(k)

MENSTRUAL PADS

K-Number: K834564 · 1984-03-30

Decision Date1984-03-30
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MENSTRUAL PADS is the device name listed in this FDA 510(k) record. The listed applicant is Probel-U.S., Inc.. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K834564. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENSTRUAL PADS?

MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Probel-U.S., Inc.. The 510(k) number is K834564.

When did MENSTRUAL PADS receive FDA 510(k) clearance?

MENSTRUAL PADS received FDA 510(k) clearance on 1984-03-30, under 510(k) number K834564.

Who is the listed applicant for MENSTRUAL PADS?

The FDA 510(k) record lists Probel-U.S., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENSTRUAL PADS?

The FDA product code for MENSTRUAL PADS 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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