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FDA 510(k)

Y CONNECTOR

K-Number: K851921 · 1985-05-17

ApplicantSil-Med Corp.
Decision Date1985-05-17
Product CodeGCD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Y CONNECTOR 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 1985-05-17 under 510(k) number K851921. The device is classified under product code GCD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Y CONNECTOR?

Y CONNECTOR is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Sil-Med Corp.. The 510(k) number is K851921.

When did Y CONNECTOR receive FDA 510(k) clearance?

Y CONNECTOR received FDA 510(k) clearance on 1985-05-17, under 510(k) number K851921.

Who is the listed applicant for Y CONNECTOR?

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 Y CONNECTOR?

The FDA product code for Y CONNECTOR is GCD.

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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: GCD)

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.

K952470ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.R-Group Intl.K940198L-CATH CONNECTOR ASSEMBLYLuther Medical Products, Inc.K863446ANGIOMED HIGH PRESSURE CONNECTORSAngiomed U.S., Inc.K851196INCISION DRAINSil-Med Corp.K760382CONNECTORSB. Braun InstrumentsK760524CATHETER CONNECTOR, ARGYLE TUBINGSherwood Medical Industries

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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