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FDA 510(k)

QUINTON INJECTION SEALING CAP

K-Number: K844193 · 1985-05-17

ApplicantQuinton, Inc.
Decision Date1985-05-17
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

QUINTON INJECTION SEALING CAP is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1985-05-17 under 510(k) number K844193. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUINTON INJECTION SEALING CAP?

QUINTON INJECTION SEALING CAP is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Quinton, Inc.. The 510(k) number is K844193.

When did QUINTON INJECTION SEALING CAP receive FDA 510(k) clearance?

QUINTON INJECTION SEALING CAP received FDA 510(k) clearance on 1985-05-17, under 510(k) number K844193.

Who is the listed applicant for QUINTON INJECTION SEALING CAP?

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 QUINTON INJECTION SEALING CAP?

The FDA product code for QUINTON INJECTION SEALING CAP is FOZ.

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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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Related Devices (Code: FOZ)

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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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