GARDS (UNSCENTED, MENSTRUAL PAD)
K-Number: K822433 · 1982-08-30
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Device Summary
Frequently Asked Questions
What is the GARDS (UNSCENTED, MENSTRUAL PAD)?
GARDS (UNSCENTED, MENSTRUAL PAD) is a medical device that received FDA 510(k) clearance on 1982-08-30. The listed applicant is Hospital Specialty Co.. The 510(k) number is K822433.
When did GARDS (UNSCENTED, MENSTRUAL PAD) receive FDA 510(k) clearance?
GARDS (UNSCENTED, MENSTRUAL PAD) received FDA 510(k) clearance on 1982-08-30, under 510(k) number K822433.
Who is the listed applicant for GARDS (UNSCENTED, MENSTRUAL PAD)?
The FDA 510(k) record lists Hospital Specialty Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GARDS (UNSCENTED, MENSTRUAL PAD)?
The FDA product code for GARDS (UNSCENTED, MENSTRUAL PAD) 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 Hospital Specialty Co. 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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