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FDA 510(k)

PRINCE MEDICAL CEMENT PLUG

K-Number: K981855 · 1998-08-10

ApplicantPrince Medical, Inc.
Decision Date1998-08-10
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PRINCE MEDICAL CEMENT PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Prince Medical, Inc.. It received FDA 510(k) clearance on 1998-08-10 under 510(k) number K981855. 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 PRINCE MEDICAL CEMENT PLUG?

PRINCE MEDICAL CEMENT PLUG is a medical device that received FDA 510(k) clearance on 1998-08-10. The listed applicant is Prince Medical, Inc.. The 510(k) number is K981855.

When did PRINCE MEDICAL CEMENT PLUG receive FDA 510(k) clearance?

PRINCE MEDICAL CEMENT PLUG received FDA 510(k) clearance on 1998-08-10, under 510(k) number K981855.

Who is the listed applicant for PRINCE MEDICAL CEMENT PLUG?

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

What is the FDA product code for PRINCE MEDICAL CEMENT PLUG?

The FDA product code for PRINCE MEDICAL CEMENT PLUG is 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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