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FDA 510(k)

MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM

K-Number: K874512 · 1988-01-27

ApplicantStackhouse Assoc.
Decision Date1988-01-27
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stackhouse Assoc.. It received FDA 510(k) clearance on 1988-01-27 under 510(k) number K874512. 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 MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM?

MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM is a medical device that received FDA 510(k) clearance on 1988-01-27. The listed applicant is Stackhouse Assoc.. The 510(k) number is K874512.

When did MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM receive FDA 510(k) clearance?

MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM received FDA 510(k) clearance on 1988-01-27, under 510(k) number K874512.

Who is the listed applicant for MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM?

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

What is the FDA product code for MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM?

The FDA product code for MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM is FYD.

Related Clinical Trials

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Other records listing Stackhouse Assoc. 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.

K912651AIRSAFE MINIVAC SMOKE FILTRATION SYSTEMK910515FREEDOM MARK III SURGICAL HELMET SYSTEMK872935ANTI-INFECTION SHIELDK790877BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO

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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