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510(k) K885241

BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MAT by King Mfg. Co. — Product Code FNJ

K885241 is an FDA 510(k) premarket notification submitted by King Mfg. Co. for the device "BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MAT". The FDA issued a decision of Substantially Equivalent on February 24, 1989. The device falls under product code FNJ (Bed, Manual), a Class I device regulated under 21 CFR 880.5120.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 1989
Date Received
December 21, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bed, Manual
Device Class
Class I
Regulation Number
880.5120
Review Panel
HO
Submission Type

Other clearances for product code FNJ

  • K934298 — KING KRIB (January 26, 1994)
  • K892877 — CRADLE, HOSPITAL BED CLOTHING (June 15, 1989)
  • K884542 — SIC 3999 FOLDING ADJUSTABLE HOSPITAL BED (November 21, 1988)
  • K881725 — ENVIROTENT (BED) (November 8, 1988)
  • K881961 — MSI STANDARD BED MODELS: L1097-64 AND L1085-64 (November 1, 1988)
  • K881964 — MSI 3003 SERIES BED (June 28, 1988)
  • K881962 — MSI 2005 SERIES BED (June 3, 1988)
  • K881043 — FOLDING HOSPITAL COT NSN 6530-00-299-8517 (April 12, 1988)
  • K870166 — PLATFORM MATTRESS W/DISPOSABLE BEDPAN BAG (March 13, 1987)
  • K870310 — VSID MEDICAL THREE-FOLDING BED (February 10, 1987)

FDA data resources