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FDA 510(k)

ARGYLE DOUBLE SEAL CHEST DRAINAGE UNIT

K-Number: K802891 · 1980-12-19

ApplicantSherwood Medical Co.
Decision Date1980-12-19
Product CodeCCJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARGYLE DOUBLE SEAL CHEST DRAINAGE UNIT 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 1980-12-19 under 510(k) number K802891. The device is classified under product code CCJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE DOUBLE SEAL CHEST DRAINAGE UNIT?

ARGYLE DOUBLE SEAL CHEST DRAINAGE UNIT is a medical device that received FDA 510(k) clearance on 1980-12-19. The listed applicant is Sherwood Medical Co.. The 510(k) number is K802891.

When did ARGYLE DOUBLE SEAL CHEST DRAINAGE UNIT receive FDA 510(k) clearance?

ARGYLE DOUBLE SEAL CHEST DRAINAGE UNIT received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802891.

Who is the listed applicant for ARGYLE DOUBLE SEAL CHEST DRAINAGE UNIT?

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 DOUBLE SEAL CHEST DRAINAGE UNIT?

The FDA product code for ARGYLE DOUBLE SEAL CHEST DRAINAGE UNIT is CCJ.

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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.

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Related Devices (Code: CCJ)

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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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