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FDA 510(k)

VITEX P.D.A

K-Number: K834560 · 1984-02-27

ApplicantJeneric Ind.
Decision Date1984-02-27
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VITEX P.D.A is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1984-02-27 under 510(k) number K834560. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITEX P.D.A?

VITEX P.D.A is a medical device that received FDA 510(k) clearance on 1984-02-27. The listed applicant is Jeneric Ind.. The 510(k) number is K834560.

When did VITEX P.D.A receive FDA 510(k) clearance?

VITEX P.D.A received FDA 510(k) clearance on 1984-02-27, under 510(k) number K834560.

Who is the listed applicant for VITEX P.D.A?

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

What is the FDA product code for VITEX P.D.A?

The FDA product code for VITEX P.D.A is EJH.

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Other records listing Jeneric Ind. 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.

K862822REXILLIUM N. B. F.K862926SURGICAL VITEXK854878H40 BASE METAL ALLOYK844122RX CBGK844123RX CBYK840561RX ELAN

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Related Devices (Code: EJH)

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.

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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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