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FDA 510(k)

SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN

K-Number: K926496 · 1995-05-24

ApplicantSil-Med Corp.
Decision Date1995-05-24
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN 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 1995-05-24 under 510(k) number K926496. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN?

SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is Sil-Med Corp.. The 510(k) number is K926496.

When did SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN receive FDA 510(k) clearance?

SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN received FDA 510(k) clearance on 1995-05-24, under 510(k) number K926496.

Who is the listed applicant for SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN?

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 SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN?

The FDA product code for SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN is GBX.

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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: GBX)

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.

K082725GRAFTGUARD PRESSURE CONTROLLING SYRINGEMaquet Cardiovascular, LLCK052286DEUTSCH ANTI-BLOCKAGE WOUND DRAINThe Catheter Exchange, Inc.K043515GRAFTSAVERVescare, Inc.K013417MISONIX IRRIGATION SYSTEM MOEDL BC20PMisonix, Inc.K000704DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)Dmc Medical, Ltd.K974233LYSONIX IRRIGATION SYSTEMLysonix, 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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