BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO— 510(k) K790877

Name: FDA 510(k) clearance K790877
Creator: U.S. Food and Drug Administration
Published: 1979-05-23

Substantially Equivalent

Stackhouse Assoc.

FDA 510(k) clearance K790877 for BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO, Substantially Equivalent on 1979-05-23. Applicant: Stackhouse Assoc.. Device class: 1.

Clearance details

Applicant: Stackhouse Assoc.
Product code: Code JDY
Device class: Class 1
Regulation: 21 CFR 888.4220
Advisory panel: Orthopedic
Date received: 1979-05-07
Decision date: 1979-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JDY

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K902167 — CONTAIN(TM) LASER PLUME FILTER1991-01-04
K902056 — LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER1990-10-30
K862509 — CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-0001986-07-23
K810542 — CEMENT FUME EVACUATOR TANK & FILTER1981-03-13
K780202 — MONOMER EVACUATION SYSTEM1978-02-21

More clearances from Stackhouse Assoc.

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K912651 — AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM1991-07-08
K910515 — FREEDOM MARK III SURGICAL HELMET SYSTEM1991-05-06
K874512 — MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM1988-01-27
K872935 — ANTI-INFECTION SHIELD1987-11-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.