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FDA 510(k)

PHOSPHOLIPIDS-E

K-Number: K863071 · 1986-09-09

ApplicantJ. D. Assoc.
Decision Date1986-09-09
Product CodeCEQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHOSPHOLIPIDS-E is the device name listed in this FDA 510(k) record. The listed applicant is J. D. Assoc.. It received FDA 510(k) clearance on 1986-09-09 under 510(k) number K863071. The device is classified under product code CEQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOSPHOLIPIDS-E?

PHOSPHOLIPIDS-E is a medical device that received FDA 510(k) clearance on 1986-09-09. The listed applicant is J. D. Assoc.. The 510(k) number is K863071.

When did PHOSPHOLIPIDS-E receive FDA 510(k) clearance?

PHOSPHOLIPIDS-E received FDA 510(k) clearance on 1986-09-09, under 510(k) number K863071.

Who is the listed applicant for PHOSPHOLIPIDS-E?

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

What is the FDA product code for PHOSPHOLIPIDS-E?

The FDA product code for PHOSPHOLIPIDS-E is CEQ.

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 J. D. Assoc. 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.

K863054AST S.C.E. (GOT)K863103PEG 6,000K863069MAGNESIOMETERK863079CREATINKINETICK863112PROTEINMETERK863053ALT S.C.E. (GPT)

View all 34 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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