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FDA 510(k)

ACCESS. TO INTERAVACULAR ADMIN. SET

K-Number: K842657 · 1984-08-17

ApplicantTanner Corp.
Decision Date1984-08-17
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACCESS. TO INTERAVACULAR ADMIN. SET is the device name listed in this FDA 510(k) record. The listed applicant is Tanner Corp.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842657. 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 ACCESS. TO INTERAVACULAR ADMIN. SET?

ACCESS. TO INTERAVACULAR ADMIN. SET is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Tanner Corp.. The 510(k) number is K842657.

When did ACCESS. TO INTERAVACULAR ADMIN. SET receive FDA 510(k) clearance?

ACCESS. TO INTERAVACULAR ADMIN. SET received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842657.

Who is the listed applicant for ACCESS. TO INTERAVACULAR ADMIN. SET?

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

What is the FDA product code for ACCESS. TO INTERAVACULAR ADMIN. SET?

The FDA product code for ACCESS. TO INTERAVACULAR ADMIN. 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.

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

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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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