Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GARDS DEODORANT SANITARY NAPKIN

K-Number: K882094 · 1988-09-22

Decision Date1988-09-22
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GARDS DEODORANT SANITARY NAPKIN is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Specialty Co.. It received FDA 510(k) clearance on 1988-09-22 under 510(k) number K882094. 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 GARDS DEODORANT SANITARY NAPKIN?

GARDS DEODORANT SANITARY NAPKIN is a medical device that received FDA 510(k) clearance on 1988-09-22. The listed applicant is Hospital Specialty Co.. The 510(k) number is K882094.

When did GARDS DEODORANT SANITARY NAPKIN receive FDA 510(k) clearance?

GARDS DEODORANT SANITARY NAPKIN received FDA 510(k) clearance on 1988-09-22, under 510(k) number K882094.

Who is the listed applicant for GARDS DEODORANT SANITARY NAPKIN?

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 DEODORANT SANITARY NAPKIN?

The FDA product code for GARDS DEODORANT SANITARY NAPKIN 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 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.

View all 7 devices →

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.

↑