POWERMATIC EXAMINATION TABLE— 510(k) K933577

Name: FDA 510(k) clearance K933577
Creator: U.S. Food and Drug Administration
Published: 1993-09-30

Substantially Equivalent

Medical Device Inspection Co., Inc.

FDA 510(k) clearance K933577 for POWERMATIC EXAMINATION TABLE, Substantially Equivalent on 1993-09-30. Applicant: Medical Device Inspection Co., Inc.. Device class: 1.

Clearance details

Applicant: Medical Device Inspection Co., Inc.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1993-07-22
Decision date: 1993-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code INQ

view all

K960332 — CARDON PHYSICAL THERAPY TABLE MODEL R285981996-02-13
K960334 — CARDON PHYSICAL THERAPY TABLE MODEL R271161996-02-13
K960336 — CARDON PHYSICAL THERAPY TABLE MODEL R276451996-02-13
K960196 — TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 7771996-02-07
K953621 — EVT-33001995-11-14

More clearances from Medical Device Inspection Co., Inc.

view all

K945826 — J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONS1995-08-04
K932072 — JARIT SURGICAL INSTRUMENTS1994-01-11
K931594 — THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM1993-12-21
K933578 — POWERMATIC MAT PLATFORM1993-11-05
K933580 — POWER WORK TABLE1993-11-05

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