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510(k) K881960

MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74 by Med Service, Inc. — Product Code FNL

K881960 is an FDA 510(k) premarket notification submitted by Med Service, Inc. for the device "MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74". The FDA issued a decision of Substantially Equivalent on November 1, 1988. The device falls under product code FNL (Bed, Ac-Powered Adjustable Hospital), a Class II device regulated under 21 CFR 880.5100. Med Service, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 1, 1988
Date Received
May 10, 1988
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 Med Service, Inc.

  • K881961 — MSI STANDARD BED MODELS: L1097-64 AND L1085-64 (November 1, 1988)
  • K881782 — MSI 4000 SERIES BED (July 12, 1988)
  • K881964 — MSI 3003 SERIES BED (June 28, 1988)
  • K881963 — MSI 3002 SERIES BED (June 28, 1988)
  • K881962 — MSI 2005 SERIES BED (June 3, 1988)
  • K881965 — MSI 5000 SERIES BED (May 31, 1988)
  • K881027 — MSI 2002 SERIES BED (May 26, 1988)
  • K873291 — MSI 9000 SERIES BED (December 30, 1987)

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