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FDA 510(k)

INTERFACE - CAVITY LINER

K-Number: K897130 · 1990-03-27

ApplicantScientific Pharmaceuticals, Inc.
Decision Date1990-03-27
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERFACE - CAVITY LINER is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1990-03-27 under 510(k) number K897130. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERFACE - CAVITY LINER?

INTERFACE - CAVITY LINER is a medical device that received FDA 510(k) clearance on 1990-03-27. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K897130.

When did INTERFACE - CAVITY LINER receive FDA 510(k) clearance?

INTERFACE - CAVITY LINER received FDA 510(k) clearance on 1990-03-27, under 510(k) number K897130.

Who is the listed applicant for INTERFACE - CAVITY LINER?

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

What is the FDA product code for INTERFACE - CAVITY LINER?

The FDA product code for INTERFACE - CAVITY LINER is EJK.

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Other records listing Scientific Pharmaceuticals, 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: EJK)

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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