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)

WOUND DRESSING/ABD PAD, MODEL #10810

K-Number: K990861 · 1999-04-12

Decision Date1999-04-12
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WOUND DRESSING/ABD PAD, MODEL #10810 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 1999-04-12 under 510(k) number K990861. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOUND DRESSING/ABD PAD, MODEL #10810?

WOUND DRESSING/ABD PAD, MODEL #10810 is a medical device that received FDA 510(k) clearance on 1999-04-12. The listed applicant is Hospital Specialty Co.. The 510(k) number is K990861.

When did WOUND DRESSING/ABD PAD, MODEL #10810 receive FDA 510(k) clearance?

WOUND DRESSING/ABD PAD, MODEL #10810 received FDA 510(k) clearance on 1999-04-12, under 510(k) number K990861.

Who is the listed applicant for WOUND DRESSING/ABD PAD, MODEL #10810?

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 WOUND DRESSING/ABD PAD, MODEL #10810?

The FDA product code for WOUND DRESSING/ABD PAD, MODEL #10810 is NAD.

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: NAD)

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.

↑