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FDA 510(k)

INFUSION PUMP #6202

K-Number: K771478 · 1977-08-22

ApplicantRoche Medical Electronics, Inc.
Decision Date1977-08-22
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSION PUMP #6202 is the device name listed in this FDA 510(k) record. The listed applicant is Roche Medical Electronics, Inc.. It received FDA 510(k) clearance on 1977-08-22 under 510(k) number K771478. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFUSION PUMP #6202?

INFUSION PUMP #6202 is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Roche Medical Electronics, Inc.. The 510(k) number is K771478.

When did INFUSION PUMP #6202 receive FDA 510(k) clearance?

INFUSION PUMP #6202 received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771478.

Who is the listed applicant for INFUSION PUMP #6202?

The FDA 510(k) record lists Roche Medical Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INFUSION PUMP #6202?

The FDA product code for INFUSION PUMP #6202 is FRN.

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Other records listing Roche Medical Electronics, Inc. as applicant

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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.

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