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510(k) K922119

MODEL 5002 LIFT WEIGH-SCALE by Acme Medical Scale Co. — Product Code FRW

K922119 is an FDA 510(k) premarket notification submitted by Acme Medical Scale Co. for the device "MODEL 5002 LIFT WEIGH-SCALE". The FDA issued a decision of Substantially Equivalent on February 3, 1993. The device falls under product code FRW (Scale, Patient), a Class I device regulated under 21 CFR 880.2720. Acme Medical Scale Co. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 3, 1993
Date Received
May 5, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scale, Patient
Device Class
Class I
Regulation Number
880.2720
Review Panel
HO
Submission Type

Other clearances by Acme Medical Scale Co.

  • K926174 — MODEL 9100 H.R. INFANT SCALE (October 25, 1993)
  • K910055 — ACME MODEL 8500 WHEELCHAIR SCALE (January 14, 1991)
  • K852278 — ACME(BRAND) LOW-PROFILE WHEELCHAIR SCALE, 17400 (June 7, 1985)
  • K851014 — ACME LOW-PROFILE CHAIR SCAL 7300 (March 27, 1985)
  • K841534 — ACME DIGITAL INFANT SCALE-30 (May 31, 1984)
  • K830171 — DIGITAL BEDSIDE SCALE #5000 (February 18, 1983)
  • K790130 — SCALE, DIGITAL CHAIR (February 1, 1979)
  • K781832 — SCALE, ACME DIGITAL BEDSIDE (December 7, 1978)
  • K760327 — WHEEL'N WEIGH (October 20, 1976)

Other clearances for product code FRW

  • K955357 — OLYMPIC SMART SCALE MODEL 50/50RA (January 30, 1996)
  • K955177 — OLYMPIC SMART SCALE (December 14, 1995)
  • K954846 — OLYMPIC SMART SCALE (December 14, 1995)
  • K952649 — WARM-SCALE (August 15, 1995)
  • K943587 — ADVANCED IN-BED WEIGH SYSTEM (September 22, 1994)
  • K932572 — DIGITAL BABY SCALE MODEL BLB-12 (November 16, 1993)
  • K926174 — MODEL 9100 H.R. INFANT SCALE (October 25, 1993)
  • K926446 — EZ PUMP (September 27, 1993)
  • K926059 — 3M MODEL 200RT RATE TAPER INFUSION PUMP (August 16, 1993)
  • K926058 — 3M MODEL 280RT RATE TAPER INFUSION PUMP (August 16, 1993)

FDA data resources