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FDA 510(k)

DOW CORNING/W RIGHT WOUND DRAINAGE SYS

K-Number: K800014 · 1980-01-17

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1980-01-17
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DOW CORNING/W RIGHT WOUND DRAINAGE SYS is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. It received FDA 510(k) clearance on 1980-01-17 under 510(k) number K800014. 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 DOW CORNING/W RIGHT WOUND DRAINAGE SYS?

DOW CORNING/W RIGHT WOUND DRAINAGE SYS is a medical device that received FDA 510(k) clearance on 1980-01-17. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K800014.

When did DOW CORNING/W RIGHT WOUND DRAINAGE SYS receive FDA 510(k) clearance?

DOW CORNING/W RIGHT WOUND DRAINAGE SYS received FDA 510(k) clearance on 1980-01-17, under 510(k) number K800014.

Who is the listed applicant for DOW CORNING/W RIGHT WOUND DRAINAGE SYS?

The FDA 510(k) record lists Dow Corning Corp. Healthcare Industries Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOW CORNING/W RIGHT WOUND DRAINAGE SYS?

The FDA product code for DOW CORNING/W RIGHT WOUND DRAINAGE SYS is GCY.

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Other records listing Dow Corning Corp. Healthcare Industries Materials 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.

K853186SILASTIC INFLATABLE BONE PLUG H.P.K844637WHITESIDE ACRYLIC CEMENT SPACER SLEEVEK850255DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMETK843995TF-II HIP PROSTHESISK842559WHITESIDE ORTHOLOC TOTAL HIP FEMORALK840357SSA HIP PROSTHESIS

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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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