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FDA 510(k)

T-TYPE IV EXTENSION SET

K-Number: K843249 · 1984-09-07

Decision Date1984-09-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

T-TYPE IV EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Strato Medical Corp.. It received FDA 510(k) clearance on 1984-09-07 under 510(k) number K843249. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-TYPE IV EXTENSION SET?

T-TYPE IV EXTENSION SET is a medical device that received FDA 510(k) clearance on 1984-09-07. The listed applicant is Strato Medical Corp.. The 510(k) number is K843249.

When did T-TYPE IV EXTENSION SET receive FDA 510(k) clearance?

T-TYPE IV EXTENSION SET received FDA 510(k) clearance on 1984-09-07, under 510(k) number K843249.

Who is the listed applicant for T-TYPE IV EXTENSION SET?

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

What is the FDA product code for T-TYPE IV EXTENSION SET?

The FDA product code for T-TYPE IV EXTENSION SET is FPA.

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 Strato Medical Corp. 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.

View all 45 devices →

Related Devices (Code: FPA)

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

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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