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510(k) K882010

POWER EXAMINATION TABLE by Enochs Mfg., Inc. — Product Code LGX

K882010 is an FDA 510(k) premarket notification submitted by Enochs Mfg., Inc. for the device "POWER EXAMINATION TABLE". The FDA issued a decision of Substantially Equivalent on July 13, 1988. The device falls under product code LGX (Table, Examination, Medical, Powered), a Class I device regulated under 21 CFR 878.4960.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 13, 1988
Date Received
May 13, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Examination, Medical, Powered
Device Class
Class I
Regulation Number
878.4960
Review Panel
HO
Submission Type

Other clearances for product code LGX

  • K945163 — ECHOCARDIOGRAPHY (February 17, 1995)
  • K894134 — POWER EXAMINATION TABLE MODEL # 411 (August 28, 1989)
  • K894144 — POWER EXAMINATION TABLE MODEL # 405 (August 28, 1989)
  • K883680 — MEDALIST EXAMINATION TABLE (October 4, 1988)
  • K864072 — ADEC 1005-C CHAIR (November 7, 1986)
  • K860519 — RELIANCE MODEL 200 PODIATRY CHAIR (February 19, 1986)
  • K845023 — STORZ PLASTIC SURGERY & EXAMINATION LOUNGE 7000 (January 28, 1985)
  • K830294 — MEDICAL EXAM TABLE (January 11, 1984)
  • K832768 — S & W SW52E W/POWER BACK LIFT (September 20, 1983)
  • K820823 — MULTIPLE, MODEL #17 (April 21, 1982)

FDA data resources