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FDA 510(k)

CATHETEO CARE TRAY #0242

K-Number: K771673 · 1977-09-30

ApplicantConcord Laboratories, Inc.
Decision Date1977-09-30
Product CodeFMC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATHETEO CARE TRAY #0242 is the device name listed in this FDA 510(k) record. The listed applicant is Concord Laboratories, Inc.. It received FDA 510(k) clearance on 1977-09-30 under 510(k) number K771673. The device is classified under product code FMC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETEO CARE TRAY #0242?

CATHETEO CARE TRAY #0242 is a medical device that received FDA 510(k) clearance on 1977-09-30. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K771673.

When did CATHETEO CARE TRAY #0242 receive FDA 510(k) clearance?

CATHETEO CARE TRAY #0242 received FDA 510(k) clearance on 1977-09-30, under 510(k) number K771673.

Who is the listed applicant for CATHETEO CARE TRAY #0242?

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

What is the FDA product code for CATHETEO CARE TRAY #0242?

The FDA product code for CATHETEO CARE TRAY #0242 is FMC.

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Other records listing Concord Laboratories, 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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