FDA 510(k)

MILK BATH CONCENTRATE

K-Number: K780258 · 1978-06-13

Decision Date1978-06-13

Product Code

DecisionSubstantially Equivalent

Device Summary

MILK BATH CONCENTRATE is the device name listed in this FDA 510(k) record. The listed applicant is Sparta Instrument Corp.. It received FDA 510(k) clearance on 1978-06-13 under 510(k) number K780258. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILK BATH CONCENTRATE?

MILK BATH CONCENTRATE is a medical device that received FDA 510(k) clearance on 1978-06-13. The listed applicant is Sparta Instrument Corp.. The 510(k) number is K780258.

When did MILK BATH CONCENTRATE receive FDA 510(k) clearance?

MILK BATH CONCENTRATE received FDA 510(k) clearance on 1978-06-13, under 510(k) number K780258.

Who is the listed applicant for MILK BATH CONCENTRATE?

The FDA 510(k) record lists Sparta Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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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Other records listing Sparta Instrument Corp. as applicant

K854475GHAJAR INTRAVENTRICULAR CATHETER GUIDE K781365SPARTA BRONCHIAL BRUSH K780257MICROSPEARS

Official Source

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