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FDA 510(k)

ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL

K-Number: K871265 · 1987-08-13

Decision Date1987-08-13
Product CodeLBS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1987-08-13 under 510(k) number K871265. The device is classified under product code LBS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL?

ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL is a medical device that received FDA 510(k) clearance on 1987-08-13. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K871265.

When did ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL receive FDA 510(k) clearance?

ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL received FDA 510(k) clearance on 1987-08-13, under 510(k) number K871265.

Who is the listed applicant for ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL?

The FDA product code for ANALYST(TM) LIPID ROTOR & HDL CALIBRATOR/CONTROL is LBS.

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 E.I. Dupont DE Nemours & Co., 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.

View all 253 devices →

Related Devices (Code: LBS)

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

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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