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510(k) K903904

SERIES 2000 ADJUSTABLE BED by Equi-Tron Mfg., Inc. — Product Code FNL

K903904 is an FDA 510(k) premarket notification submitted by Equi-Tron Mfg., Inc. for the device "SERIES 2000 ADJUSTABLE BED". The FDA issued a decision of Substantially Equivalent on October 12, 1990. The device falls under product code FNL (Bed, Ac-Powered Adjustable Hospital), a Class II device regulated under 21 CFR 880.5100. Equi-Tron Mfg., Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 12, 1990
Date Received
August 23, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bed, Ac-Powered Adjustable Hospital
Device Class
Class II
Regulation Number
880.5100
Review Panel
HO
Submission Type

Other clearances by Equi-Tron Mfg., Inc.

  • K962763 — 2000 MODULAR THIRTY-NINE (October 7, 1996)
  • K903905 — SERIES 9000 LIFT-RECLINE CHAIR (September 17, 1990)
  • K902089 — EQUI-GUARD (ASPIRATOR FILTER) (July 6, 1990)
  • K894831 — PORTABLE AIR COMPRESSOR MODEL NUMBER 8125 (October 24, 1989)

Other clearances for product code FNL

  • K202964 — iBed Wireless with iBed Mobile (June 18, 2021)
  • K103536 — IBED WIRELESS WITH IBED AWARENESS (December 16, 2010)
  • K982783 — VAIL 1000 ENCLOSED BED (October 5, 1998)
  • K974296 — MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED (January 6, 1998)
  • K974254 — BENEFIT B3--- SERIES (December 16, 1997)
  • K972115 — VOLKER HOSPITAL BED, MODEL K960 (August 29, 1997)
  • K971546 — SOMA 900 TRANSPORT BED (July 10, 1997)
  • K963622 — VAIL 2000 ENCLOSED BED (May 7, 1997)
  • K963589 — VAIL 3000 BED ENCLOSURE (April 21, 1997)
  • K962942 — TOTALCARE (February 3, 1997)

FDA data resources