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FDA 510(k)

CRF CHARCOAL CANISTER REPLACEMENT FILTER

K-Number: K920209 · 1992-10-01

ApplicantQuinn Healthcare Products
Decision Date1992-10-01
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CRF CHARCOAL CANISTER REPLACEMENT FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Quinn Healthcare Products. It received FDA 510(k) clearance on 1992-10-01 under 510(k) number K920209. 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 CRF CHARCOAL CANISTER REPLACEMENT FILTER?

CRF CHARCOAL CANISTER REPLACEMENT FILTER is a medical device that received FDA 510(k) clearance on 1992-10-01. The listed applicant is Quinn Healthcare Products. The 510(k) number is K920209.

When did CRF CHARCOAL CANISTER REPLACEMENT FILTER receive FDA 510(k) clearance?

CRF CHARCOAL CANISTER REPLACEMENT FILTER received FDA 510(k) clearance on 1992-10-01, under 510(k) number K920209.

Who is the listed applicant for CRF CHARCOAL CANISTER REPLACEMENT FILTER?

The FDA 510(k) record lists Quinn Healthcare Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRF CHARCOAL CANISTER REPLACEMENT FILTER?

The FDA product code for CRF CHARCOAL CANISTER REPLACEMENT FILTER is FYD.

Related Clinical Trials

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.

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Other records listing Quinn Healthcare Products 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.

K920210SRH-678 VACCUUM TUBING

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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