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FDA 510(k)

ARGYLE VAC-U-CARE 100CC SUCTION RESERV

K-Number: K821563 · 1982-06-21

ApplicantSherwood Medical Co.
Decision Date1982-06-21
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARGYLE VAC-U-CARE 100CC SUCTION RESERV 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 1982-06-21 under 510(k) number K821563. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE VAC-U-CARE 100CC SUCTION RESERV?

ARGYLE VAC-U-CARE 100CC SUCTION RESERV is a medical device that received FDA 510(k) clearance on 1982-06-21. The listed applicant is Sherwood Medical Co.. The 510(k) number is K821563.

When did ARGYLE VAC-U-CARE 100CC SUCTION RESERV receive FDA 510(k) clearance?

ARGYLE VAC-U-CARE 100CC SUCTION RESERV received FDA 510(k) clearance on 1982-06-21, under 510(k) number K821563.

Who is the listed applicant for ARGYLE VAC-U-CARE 100CC SUCTION RESERV?

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 VAC-U-CARE 100CC SUCTION RESERV?

The FDA product code for ARGYLE VAC-U-CARE 100CC SUCTION RESERV is GCY.

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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: GCY)

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.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, Inc.

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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