PLASTER VACUUM, 115V MODEL NO. 4183-160— 510(k) K873721

Name: FDA 510(k) clearance K873721
Creator: U.S. Food and Drug Administration
Published: 1987-12-07

Substantially Equivalent

Martin Medical

FDA 510(k) clearance K873721 for PLASTER VACUUM, 115V MODEL NO. 4183-160, Substantially Equivalent on 1987-12-07. Applicant: Martin Medical. Device class: 1.

Clearance details

Applicant: Martin Medical
Product code: Code LGH
Device class: Class 1
Regulation: 21 CFR 888.5960
Advisory panel: Orthopedic
Date received: 1987-09-15
Decision date: 1987-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Desoto, KS, US

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K873723 — PLASTER VACUUM, 230V MODEL NO. 4183-1611987-12-10

More clearances from Martin Medical

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K873716 — ADULT WALKING HEEL PRODUCT NO. 4183-1301987-10-02
K873717 — CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-1351987-10-02
K873718 — CHILD WALKING HEEL PRODUCT NO. 4183-1321987-10-02
K873719 — CAST CUTTER, 115V MODEL NO. 4183-1061987-10-02
K873720 — CAST CUTTER, 230V MODEL NO. 4183-1071987-10-02

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