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FDA 510(k)

ULTRACHEM TOTAL PROTEIN, #64974

K-Number: K772155 · 1977-12-06

ApplicantHarleco
Decision Date1977-12-06
Product CodeCEK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ULTRACHEM TOTAL PROTEIN, #64974 is the device name listed in this FDA 510(k) record. The listed applicant is Harleco. It received FDA 510(k) clearance on 1977-12-06 under 510(k) number K772155. The device is classified under product code CEK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRACHEM TOTAL PROTEIN, #64974?

ULTRACHEM TOTAL PROTEIN, #64974 is a medical device that received FDA 510(k) clearance on 1977-12-06. The listed applicant is Harleco. The 510(k) number is K772155.

When did ULTRACHEM TOTAL PROTEIN, #64974 receive FDA 510(k) clearance?

ULTRACHEM TOTAL PROTEIN, #64974 received FDA 510(k) clearance on 1977-12-06, under 510(k) number K772155.

Who is the listed applicant for ULTRACHEM TOTAL PROTEIN, #64974?

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

What is the FDA product code for ULTRACHEM TOTAL PROTEIN, #64974?

The FDA product code for ULTRACHEM TOTAL PROTEIN, #64974 is CEK.

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.

Other records listing Harleco 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.

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Related Devices (Code: CEK)

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.

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.

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