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FDA 510(k)

LDC CONSTAMETRIC III HIGHT PRESS. SOL.

K-Number: K800048 · 1980-01-29

ApplicantLaboratory Data Control
Decision Date1980-01-29
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LDC CONSTAMETRIC III HIGHT PRESS. SOL. is the device name listed in this FDA 510(k) record. The listed applicant is Laboratory Data Control. It received FDA 510(k) clearance on 1980-01-29 under 510(k) number K800048. The device is classified under product code KIE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LDC CONSTAMETRIC III HIGHT PRESS. SOL.?

LDC CONSTAMETRIC III HIGHT PRESS. SOL. is a medical device that received FDA 510(k) clearance on 1980-01-29. The listed applicant is Laboratory Data Control. The 510(k) number is K800048.

When did LDC CONSTAMETRIC III HIGHT PRESS. SOL. receive FDA 510(k) clearance?

LDC CONSTAMETRIC III HIGHT PRESS. SOL. received FDA 510(k) clearance on 1980-01-29, under 510(k) number K800048.

Who is the listed applicant for LDC CONSTAMETRIC III HIGHT PRESS. SOL.?

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

What is the FDA product code for LDC CONSTAMETRIC III HIGHT PRESS. SOL.?

The FDA product code for LDC CONSTAMETRIC III HIGHT PRESS. SOL. is KIE.

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 Laboratory Data Control 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.

K800289LDC SPECTROMONITOR IIIK800046LDC CHROMATOGRAPHY ACCESSORY MODULE BK800047LDC UVIII FIXED WAVELENGTH ULTRAVIOLET

Related Devices (Code: KIE)

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.

K964588WATERS 515 HPLC PUMP (515)Waters CorporationK935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPThe Perkin-Elmer Corp.K924347WATERS(TM) 996 PDAMillipore Corp.K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.K911299EQUIPMENT/MATERIAL DECONTAMINATING KITRohm and Haas Co.K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore Corp.

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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