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FDA 510(k)

SQC BUFFER

K-Number: K812601 · 1981-10-02

ApplicantTransidyne General Corp.
Decision Date1981-10-02
Product CodeJJS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SQC BUFFER is the device name listed in this FDA 510(k) record. The listed applicant is Transidyne General Corp.. It received FDA 510(k) clearance on 1981-10-02 under 510(k) number K812601. The device is classified under product code JJS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SQC BUFFER?

SQC BUFFER is a medical device that received FDA 510(k) clearance on 1981-10-02. The listed applicant is Transidyne General Corp.. The 510(k) number is K812601.

When did SQC BUFFER receive FDA 510(k) clearance?

SQC BUFFER received FDA 510(k) clearance on 1981-10-02, under 510(k) number K812601.

Who is the listed applicant for SQC BUFFER?

The FDA 510(k) record lists Transidyne General Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SQC BUFFER?

The FDA product code for SQC BUFFER is JJS.

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Other records listing Transidyne General Corp. as applicant

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Related Devices (Code: JJS)

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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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