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FDA 510(k)

TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM

K-Number: K837142 · 1983-03-23

ApplicantHoffrel Instruments, Inc.
Decision Date1983-03-23
Product Code
DecisionSubstantially Equivalent

Device Summary

TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM 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 1983-03-23 under 510(k) number K837142. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM?

TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM is a medical device that received FDA 510(k) clearance on 1983-03-23. The listed applicant is Hoffrel Instruments, Inc.. The 510(k) number is K837142.

When did TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM receive FDA 510(k) clearance?

TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM received FDA 510(k) clearance on 1983-03-23, under 510(k) number K837142.

Who is the listed applicant for TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM?

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

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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 TRANSDUCERK850165MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417K844916MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLERK834276MOD 456K834277MOD 427

View all 12 devices →

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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