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FDA 510(k)

PERMARIDGE SYRINGE

K-Number: K962838 · 1996-08-20

ApplicantCeramed Corp.
Decision Date1996-08-20
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERMARIDGE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Ceramed Corp.. It received FDA 510(k) clearance on 1996-08-20 under 510(k) number K962838. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERMARIDGE SYRINGE?

PERMARIDGE SYRINGE is a medical device that received FDA 510(k) clearance on 1996-08-20. The listed applicant is Ceramed Corp.. The 510(k) number is K962838.

When did PERMARIDGE SYRINGE receive FDA 510(k) clearance?

PERMARIDGE SYRINGE received FDA 510(k) clearance on 1996-08-20, under 510(k) number K962838.

Who is the listed applicant for PERMARIDGE SYRINGE?

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

What is the FDA product code for PERMARIDGE SYRINGE?

The FDA product code for PERMARIDGE SYRINGE is LYC.

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Other records listing Ceramed Corp. 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.

K962786OSTEOGRAF STAINLESS STEEL SYRINGK960348OSTEOGRAF/N-300 HYDROXYLAPATITEK960353OSTEOGRAF/LD-300 HYDROXYLAPATITEK960368OSTEOGRAFT/N-700 HYDROXYLAPTITEK960361PERMAMESH-D HYDROXYLAPATITE MATRIXK960362PERMAMESH HYDROXYLAPATITE MATRIX

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Related Devices (Code: LYC)

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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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