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FDA 510(k)

ALSITE MAGNIVISION

K-Number: K772228 · 1978-01-03

ApplicantAl Nyman & Son, Inc.
Decision Date1978-01-03
Product Code
DecisionSubstantially Equivalent

Device Summary

ALSITE MAGNIVISION is the device name listed in this FDA 510(k) record. The listed applicant is Al Nyman & Son, Inc.. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K772228. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALSITE MAGNIVISION?

ALSITE MAGNIVISION is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Al Nyman & Son, Inc.. The 510(k) number is K772228.

When did ALSITE MAGNIVISION receive FDA 510(k) clearance?

ALSITE MAGNIVISION received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772228.

Who is the listed applicant for ALSITE MAGNIVISION?

The FDA 510(k) record lists Al Nyman & Son, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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.

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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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