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FDA 510(k)

BETA-CAP II

K-Number: K801679 · 1980-10-03

ApplicantQuinton, Inc.
Decision Date1980-10-03
Product CodeFJS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BETA-CAP II is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K801679. The device is classified under product code FJS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BETA-CAP II?

BETA-CAP II is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Quinton, Inc.. The 510(k) number is K801679.

When did BETA-CAP II receive FDA 510(k) clearance?

BETA-CAP II received FDA 510(k) clearance on 1980-10-03, under 510(k) number K801679.

Who is the listed applicant for BETA-CAP II?

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 BETA-CAP II?

The FDA product code for BETA-CAP II is FJS.

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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