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FDA 510(k)

CONSENSUS APEX DOME HOLE PLUG

K-Number: K960340 · 1996-03-15

ApplicantU.S. Medical Products, Inc.
Decision Date1996-03-15
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONSENSUS APEX DOME HOLE PLUG is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Medical Products, Inc.. It received FDA 510(k) clearance on 1996-03-15 under 510(k) number K960340. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSENSUS APEX DOME HOLE PLUG?

CONSENSUS APEX DOME HOLE PLUG is a medical device that received FDA 510(k) clearance on 1996-03-15. The listed applicant is U.S. Medical Products, Inc.. The 510(k) number is K960340.

When did CONSENSUS APEX DOME HOLE PLUG receive FDA 510(k) clearance?

CONSENSUS APEX DOME HOLE PLUG received FDA 510(k) clearance on 1996-03-15, under 510(k) number K960340.

Who is the listed applicant for CONSENSUS APEX DOME HOLE PLUG?

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

What is the FDA product code for CONSENSUS APEX DOME HOLE PLUG?

The FDA product code for CONSENSUS APEX DOME HOLE PLUG is JDI.

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Other records listing U.S. Medical Products, 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.

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Related Devices (Code: JDI)

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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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