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FDA 510(k)

MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417

K-Number: K850165 · 1985-10-23

ApplicantHoffrel Instruments, Inc.
Decision Date1985-10-23
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417 is the device name listed in this FDA 510(k) record. The listed applicant is Hoffrel Instruments, Inc.. It received FDA 510(k) clearance on 1985-10-23 under 510(k) number K850165. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417?

MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417 is a medical device that received FDA 510(k) clearance on 1985-10-23. The listed applicant is Hoffrel Instruments, Inc.. The 510(k) number is K850165.

When did MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417 receive FDA 510(k) clearance?

MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417 received FDA 510(k) clearance on 1985-10-23, under 510(k) number K850165.

Who is the listed applicant for MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417?

The FDA 510(k) record lists Hoffrel Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417?

The FDA product code for MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417 is JOP.

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Other records listing Hoffrel Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K870850MOD 482K860235MOD 426, MEDICAL ULTRASONIC DIAGNOSTC TRANSDUCERK844916MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLERK834277MOD 427K834276MOD 456K837282MODEL VPS VASCULAR PROFILE SYSTEM

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Related Devices (Code: JOP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242662Falcon/Xpress (Falcon/Xpress)Viasonix , Ltd.K233976VasoGuard (V10, V8, V6, V4, V2)Corvascular Diagnostics, LLCK153762Smartdop XT6Koven Technology, Inc.K131860VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDINGUs Vascular, LLCK111416FALCONViasonix , Ltd.K071730STUDIODOP VICORDERSkidmore Medical, Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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