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FDA 510(k)

PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM

K-Number: K924732 · 1993-09-13

Decision Date1993-09-13
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Buffalo Filter Co., Inc.. It received FDA 510(k) clearance on 1993-09-13 under 510(k) number K924732. 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 PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM?

PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM is a medical device that received FDA 510(k) clearance on 1993-09-13. The listed applicant is Buffalo Filter Co., Inc.. The 510(k) number is K924732.

When did PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM receive FDA 510(k) clearance?

PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM received FDA 510(k) clearance on 1993-09-13, under 510(k) number K924732.

Who is the listed applicant for PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM?

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

What is the FDA product code for PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM?

The FDA product code for PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM 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.

Other records listing Buffalo Filter Co., Inc. 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.

View all 21 devices →

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.

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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