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510(k) K837282

MODEL VPS VASCULAR PROFILE SYSTEM by Hoffrel Instruments, Inc.

K837282 is an FDA 510(k) premarket notification submitted by Hoffrel Instruments, Inc. for the device "MODEL VPS VASCULAR PROFILE SYSTEM". The FDA issued a decision of Substantially Equivalent on April 26, 1983. Hoffrel Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 26, 1983
Date Received
March 15, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Hoffrel Instruments, Inc.

  • K870850 — MOD 482 (September 8, 1987)
  • K860235 — MOD 426, MEDICAL ULTRASONIC DIAGNOSTC TRANSDUCER (May 15, 1986)
  • K850165 — MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417 (October 23, 1985)
  • K844916 — MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLER (April 22, 1985)
  • K834276 — MOD 456 (February 17, 1984)
  • K834277 — MOD 427 (February 17, 1984)
  • K837229 — TRANSDUCER MODELS 450, 451, 452, 453, 454 (April 15, 1983)
  • K837142 — TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM (March 23, 1983)
  • K800364 — ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202 (March 12, 1980)
  • K790396 — ULTRASONIC DIAGNOSTIC SYSTEM (March 21, 1979)

FDA data resources