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FDA 510(k)

PENT CAPS

K-Number: K890662 · 1989-05-09

ApplicantJeneric/Pentron, Inc.
Decision Date1989-05-09
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PENT CAPS is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric/Pentron, Inc.. It received FDA 510(k) clearance on 1989-05-09 under 510(k) number K890662. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENT CAPS?

PENT CAPS is a medical device that received FDA 510(k) clearance on 1989-05-09. The listed applicant is Jeneric/Pentron, Inc.. The 510(k) number is K890662.

When did PENT CAPS receive FDA 510(k) clearance?

PENT CAPS received FDA 510(k) clearance on 1989-05-09, under 510(k) number K890662.

Who is the listed applicant for PENT CAPS?

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

What is the FDA product code for PENT CAPS?

The FDA product code for PENT CAPS is EJJ.

Other records listing Jeneric/Pentron, Inc. as applicant

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Related Devices (Code: EJJ)

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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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