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FDA 510(k)

GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO

K-Number: K851244 · 1985-11-19

ApplicantCook, Inc.
Decision Date1985-11-19
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1985-11-19 under 510(k) number K851244. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO?

GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO is a medical device that received FDA 510(k) clearance on 1985-11-19. The listed applicant is Cook, Inc.. The 510(k) number is K851244.

When did GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO receive FDA 510(k) clearance?

GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO received FDA 510(k) clearance on 1985-11-19, under 510(k) number K851244.

Who is the listed applicant for GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO?

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

What is the FDA product code for GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO?

The FDA product code for GRECO-HARVEY SURFACTANT BONDED CATH FOR ANESTHESIO is KDQ.

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Related Devices (Code: KDQ)

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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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