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FDA 510(k)

PRESSSION, SEQUENTIAL

K-Number: K921608 · 1992-12-30

ApplicantChattanooga Group, Inc.
Decision Date1992-12-30
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESSSION, SEQUENTIAL is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1992-12-30 under 510(k) number K921608. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSSION, SEQUENTIAL?

PRESSSION, SEQUENTIAL is a medical device that received FDA 510(k) clearance on 1992-12-30. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K921608.

When did PRESSSION, SEQUENTIAL receive FDA 510(k) clearance?

PRESSSION, SEQUENTIAL received FDA 510(k) clearance on 1992-12-30, under 510(k) number K921608.

Who is the listed applicant for PRESSSION, SEQUENTIAL?

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

What is the FDA product code for PRESSSION, SEQUENTIAL?

The FDA product code for PRESSSION, SEQUENTIAL is JOW.

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Other records listing Chattanooga Group, Inc. as applicant

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Related Devices (Code: JOW)

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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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