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FDA 510(k)

TRANSDUCER MODELS 450, 451, 452, 453, 454

K-Number: K837229 · 1983-04-15

ApplicantHoffrel Instruments, Inc.
Decision Date1983-04-15
Product Code
DecisionSubstantially Equivalent

Device Summary

TRANSDUCER MODELS 450, 451, 452, 453, 454 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 1983-04-15 under 510(k) number K837229. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSDUCER MODELS 450, 451, 452, 453, 454?

TRANSDUCER MODELS 450, 451, 452, 453, 454 is a medical device that received FDA 510(k) clearance on 1983-04-15. The listed applicant is Hoffrel Instruments, Inc.. The 510(k) number is K837229.

When did TRANSDUCER MODELS 450, 451, 452, 453, 454 receive FDA 510(k) clearance?

TRANSDUCER MODELS 450, 451, 452, 453, 454 received FDA 510(k) clearance on 1983-04-15, under 510(k) number K837229.

Who is the listed applicant for TRANSDUCER MODELS 450, 451, 452, 453, 454?

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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