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510(k) K831325

NUTROMAT by Medlog GmbH Marketing Services — Product Code GBB

K831325 is an FDA 510(k) premarket notification submitted by Medlog GmbH Marketing Services for the device "NUTROMAT". The FDA issued a decision of Substantially Equivalent on June 2, 1983. The device falls under product code GBB (Chair, Surgical, Ac-Powered), a Class I device regulated under 21 CFR 878.4960. Medlog GmbH Marketing Services has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 2, 1983
Date Received
April 25, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, Surgical, Ac-Powered
Device Class
Class I
Regulation Number
878.4960
Review Panel
SU
Submission Type

Other clearances by Medlog GmbH Marketing Services

  • K832086 — USE 77 ULTRASONIC NEBULIZER (July 19, 1983)
  • K830913 — MINITROP AEROSAL, PRODOMO AEROSAL AND (May 25, 1983)
  • K813455 — PUMP & DETECTOR (January 5, 1982)
  • K810155 — DOP 84 (May 1, 1981)

Other clearances for product code GBB

  • K964102 — TENET TIBIAL FRACTURE SUPPORT (December 5, 1996)
  • K893598 — HYDRAULIC FOOT OPERATED STOOL (October 10, 1989)
  • K831385 — LITHOTOMY CHAIR #415 (June 2, 1983)
  • K822264 — NAGASHIMA SN OPERATOR'S CHAIR (October 13, 1982)
  • K822251 — EXAMINATION & TREATMENT CHAIRS (August 27, 1982)
  • K822013 — NAGASHIMA SN AUTOMATIC TREATMENT CHAIR (July 28, 1982)
  • K820636 — STORZ #6500 POWER EXAMINATION CHAIR (March 26, 1982)

FDA data resources