FDA 510(k)

CARAFE AND LINER

K-Number: K760548 · 1976-11-12

Decision Date1976-11-12

Product Code

DecisionSubstantially Equivalent

Device Summary

CARAFE AND LINER is the device name listed in this FDA 510(k) record. The listed applicant is Landmark Plastics. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760548. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARAFE AND LINER?

CARAFE AND LINER is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Landmark Plastics. The 510(k) number is K760548.

When did CARAFE AND LINER receive FDA 510(k) clearance?

CARAFE AND LINER received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760548.

Who is the listed applicant for CARAFE AND LINER?

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

Related Clinical Trials

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Other records listing Landmark Plastics as applicant

K760494BASIN, ROUND WASH K760492BASIN, LARGE OR SMALL K760495BASIN, RECTANGULAR WASH K760552THERMOMETER STAND AND DUST COVER K760497TRAY, SERVICE K760493DISH, SOAP

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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.