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FDA 510(k)

CANNULA CLAMP

K-Number: K771419 · 1977-08-26

ApplicantQuinton, Inc.
Decision Date1977-08-26
Product CodeFKC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CANNULA CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1977-08-26 under 510(k) number K771419. The device is classified under product code FKC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULA CLAMP?

CANNULA CLAMP is a medical device that received FDA 510(k) clearance on 1977-08-26. The listed applicant is Quinton, Inc.. The 510(k) number is K771419.

When did CANNULA CLAMP receive FDA 510(k) clearance?

CANNULA CLAMP received FDA 510(k) clearance on 1977-08-26, under 510(k) number K771419.

Who is the listed applicant for CANNULA CLAMP?

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

What is the FDA product code for CANNULA CLAMP?

The FDA product code for CANNULA CLAMP is FKC.

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Other records listing Quinton, Inc. 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.

K032038PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601K021906QUINTON Q-CATH, MODEL 000460K003576Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503K001492QUINTON Q-STRESS, MODEL 000483K992908Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)K990866QUINTON MEDTRACK CR PLUS TREADMILL

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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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