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FDA 510(k)

DEXTERITY PNEUMO SLEEVE SET

K-Number: K962147 · 1996-07-09

Decision Date1996-07-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DEXTERITY PNEUMO SLEEVE SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Creative Technologies, Inc.. It received FDA 510(k) clearance on 1996-07-09 under 510(k) number K962147. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXTERITY PNEUMO SLEEVE SET?

DEXTERITY PNEUMO SLEEVE SET is a medical device that received FDA 510(k) clearance on 1996-07-09. The listed applicant is Medical Creative Technologies, Inc.. The 510(k) number is K962147.

When did DEXTERITY PNEUMO SLEEVE SET receive FDA 510(k) clearance?

DEXTERITY PNEUMO SLEEVE SET received FDA 510(k) clearance on 1996-07-09, under 510(k) number K962147.

Who is the listed applicant for DEXTERITY PNEUMO SLEEVE SET?

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

What is the FDA product code for DEXTERITY PNEUMO SLEEVE SET?

The FDA product code for DEXTERITY PNEUMO SLEEVE SET is GCJ.

Related Clinical Trials

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.

Other records listing Medical Creative Technologies, 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.

Related Devices (Code: GCJ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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