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FDA 510(k)

INAMED CLOSED-WOUND DRAIN SYSTEM

K-Number: K896491 · 1990-01-08

ApplicantInamed Development Co.
Decision Date1990-01-08
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INAMED CLOSED-WOUND DRAIN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Inamed Development Co.. It received FDA 510(k) clearance on 1990-01-08 under 510(k) number K896491. 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 INAMED CLOSED-WOUND DRAIN SYSTEM?

INAMED CLOSED-WOUND DRAIN SYSTEM is a medical device that received FDA 510(k) clearance on 1990-01-08. The listed applicant is Inamed Development Co.. The 510(k) number is K896491.

When did INAMED CLOSED-WOUND DRAIN SYSTEM receive FDA 510(k) clearance?

INAMED CLOSED-WOUND DRAIN SYSTEM received FDA 510(k) clearance on 1990-01-08, under 510(k) number K896491.

Who is the listed applicant for INAMED CLOSED-WOUND DRAIN SYSTEM?

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

What is the FDA product code for INAMED CLOSED-WOUND DRAIN SYSTEM?

The FDA product code for INAMED CLOSED-WOUND DRAIN SYSTEM is GCY.

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Other records listing Inamed Development 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.

K931548INAMED DEVELOPMENT ASPIRATION TIPK904265INAMED RUIZ-COHEN INTRAOPERATIVE TISSUE EXPANDERK901764INAMED CONVERTIBLE DRAIN SYSTEMK901742INAMED SMALL DRAIN SYSTEMK894618INAMED RHEMO-D (TM) DILATORK894073INAMED PRO-TEC SILICONE SURGICAL GLOVES

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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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