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)

ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM

K-Number: K955831 · 1996-03-28

Decision Date1996-03-28
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1996-03-28 under 510(k) number K955831. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM?

ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM is a medical device that received FDA 510(k) clearance on 1996-03-28. The listed applicant is Sherwood Medical Co.. The 510(k) number is K955831.

When did ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM receive FDA 510(k) clearance?

ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM received FDA 510(k) clearance on 1996-03-28, under 510(k) number K955831.

Who is the listed applicant for ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM?

The FDA product code for ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM is BSY.

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 Sherwood Medical 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 191 devices →

Related Devices (Code: BSY)

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.

↑