MONOMER EVACUATION SYSTEM— 510(k) K780202

Substantially Equivalent

Medishield, Inc.

FDA 510(k) clearance K780202 for MONOMER EVACUATION SYSTEM, Substantially Equivalent on 1978-02-21. Applicant: Medishield, Inc.. Device class: 1.

Clearance details

Applicant: Medishield, Inc.
Product code: Code JDY
Device class: Class 1
Regulation: 21 CFR 888.4220
Advisory panel: Orthopedic
Date received: 1978-02-07
Decision date: 1978-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code JDY

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
K790877 — BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO1979-05-23

More clearances from Medishield, Inc.

K781103 — SPECTRASCAN1978-09-27
K780645 — HMD-2000 BATTERY-POWERED MINI-DRILL, THE1978-05-03
K780646 — AIR-PWOERED COLDRILL1978-04-28
K770161 — MICROFENESTRATED HIP REPLACEMENT COMPON.1977-01-26
K761020 — ANKLE (FREEMAN-SWANSON)1976-11-23

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