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FDA 510(k)

SMOKE EVACUATION HOSES/TUBING

K-Number: K020510 · 2002-05-03

ApplicantDm Medical, Inc.
Decision Date2002-05-03
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SMOKE EVACUATION HOSES/TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Dm Medical, Inc.. It received FDA 510(k) clearance on 2002-05-03 under 510(k) number K020510. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMOKE EVACUATION HOSES/TUBING?

SMOKE EVACUATION HOSES/TUBING is a medical device that received FDA 510(k) clearance on 2002-05-03. The listed applicant is Dm Medical, Inc.. The 510(k) number is K020510.

When did SMOKE EVACUATION HOSES/TUBING receive FDA 510(k) clearance?

SMOKE EVACUATION HOSES/TUBING received FDA 510(k) clearance on 2002-05-03, under 510(k) number K020510.

Who is the listed applicant for SMOKE EVACUATION HOSES/TUBING?

The FDA 510(k) record lists Dm Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMOKE EVACUATION HOSES/TUBING?

The FDA product code for SMOKE EVACUATION HOSES/TUBING is FYD.

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Related Devices (Code: FYD)

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.

K240127PlumeSafe X5 Smoke Management SystemConmed CorporationK2337898Q10 Surclear Smoke Plume Evacuation SystemSurnic CorporationK213068Medline Smoke Evacuation ShroudMedline Industries, Inc.K202944NEBULAE SRS Laparoscopic Surgical Smoke Removal SystemNorthgate Technologies, Inc.K200250Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF SensorMegadyne Medical Products, Inc.K192035EvaQMax Smoke Evacuation SystemBio Protech, 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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