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FDA 510(k)

SUCTION RESERVOIR

K-Number: K830607 · 1983-05-02

ApplicantSil-Med Corp.
Decision Date1983-05-02
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUCTION RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Sil-Med Corp.. It received FDA 510(k) clearance on 1983-05-02 under 510(k) number K830607. 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 SUCTION RESERVOIR?

SUCTION RESERVOIR is a medical device that received FDA 510(k) clearance on 1983-05-02. The listed applicant is Sil-Med Corp.. The 510(k) number is K830607.

When did SUCTION RESERVOIR receive FDA 510(k) clearance?

SUCTION RESERVOIR received FDA 510(k) clearance on 1983-05-02, under 510(k) number K830607.

Who is the listed applicant for SUCTION RESERVOIR?

The FDA 510(k) record lists Sil-Med Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION RESERVOIR?

The FDA product code for SUCTION RESERVOIR is GCY.

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Other records listing Sil-Med Corp. 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.

K972521NAVIGATOR (STYLET) 2006K961392ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT IIK961194ANTIMICROBIAL MEDIASTINAL SILICONE DRAINK961295SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCARK960099PENROSE DRAIN MODELS 6001 - 6007K955463GRIP-A-BOOTS

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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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