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510(k) K823539

SUTTER CPM by Sutter Biomedical, Inc. — Product Code BXB

K823539 is an FDA 510(k) premarket notification submitted by Sutter Biomedical, Inc. for the device "SUTTER CPM". The FDA issued a decision of Substantially Equivalent on January 14, 1983. The device falls under product code BXB (Exerciser, Powered), a Class I device regulated under 21 CFR 890.5380. Sutter Biomedical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 14, 1983
Date Received
November 30, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Exerciser, Powered
Device Class
Class I
Regulation Number
890.5380
Review Panel
PM
Submission Type

Other clearances by Sutter Biomedical, Inc.

  • K875249 — SUTTER PHALANGEAL CAP (February 3, 1988)
  • K870200 — SUTTER FINGER JOINT PROSTHESIS (October 9, 1987)
  • K861983 — SUTTER LESSER METATARSAL CAP (September 8, 1986)
  • K850274 — SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT (April 25, 1985)
  • K830974 — SUTTER CPM 5000 (April 12, 1983)
  • K830649 — SUTTER CPM 2000 (March 17, 1983)
  • K820813 — LESSER METATARSAL PHALANG. JOINT PROSTH (May 21, 1982)
  • K820083 — SUTTER CPM (January 28, 1982)
  • K812691 — SILICONE IMPLANTS (November 16, 1981)
  • K802342 — PROXIMAL INTERPHALANGEAL JOINT IMPLANT (October 14, 1981)

Other clearances for product code BXB

  • K072887 — G-TRAINER MEDICAL (January 25, 2008)
  • K003272 — FLO-BOOT (April 4, 2001)
  • K952975 — ANKLE CALF EXERCISER PHLEBOPUMP (September 25, 1996)
  • K953456 — E-Z FLEX (January 26, 1996)
  • K955105 — BTE CPM-10 (December 29, 1995)
  • K955106 — BTE CPM-20 (December 29, 1995)
  • K951028 — HAMEX TWO (December 11, 1995)
  • K950755 — FLEXMATE K500 (October 5, 1995)
  • K951029 — HAMEX ONE (September 15, 1995)
  • K945733 — AQUAHAB, MODEL 120-72-101 (September 15, 1995)

FDA data resources