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FDA 510(k)

MODEL 617D

K-Number: K863303 · 1986-09-05

ApplicantQuinton, Inc.
Decision Date1986-09-05
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 617D is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1986-09-05 under 510(k) number K863303. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 617D?

MODEL 617D is a medical device that received FDA 510(k) clearance on 1986-09-05. The listed applicant is Quinton, Inc.. The 510(k) number is K863303.

When did MODEL 617D receive FDA 510(k) clearance?

MODEL 617D received FDA 510(k) clearance on 1986-09-05, under 510(k) number K863303.

Who is the listed applicant for MODEL 617D?

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 MODEL 617D?

The FDA product code for MODEL 617D is LDD.

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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: LDD)

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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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