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FDA 510(k)

PERLINK SCREEN, KIRAN SCREEN

K-Number: K896707 · 1990-08-30

ApplicantPerlink USA, Inc.
Decision Date1990-08-30
Product CodeEAM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PERLINK SCREEN, KIRAN SCREEN is the device name listed in this FDA 510(k) record. The listed applicant is Perlink USA, Inc.. It received FDA 510(k) clearance on 1990-08-30 under 510(k) number K896707. The device is classified under product code EAM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERLINK SCREEN, KIRAN SCREEN?

PERLINK SCREEN, KIRAN SCREEN is a medical device that received FDA 510(k) clearance on 1990-08-30. The listed applicant is Perlink USA, Inc.. The 510(k) number is K896707.

When did PERLINK SCREEN, KIRAN SCREEN receive FDA 510(k) clearance?

PERLINK SCREEN, KIRAN SCREEN received FDA 510(k) clearance on 1990-08-30, under 510(k) number K896707.

Who is the listed applicant for PERLINK SCREEN, KIRAN SCREEN?

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

What is the FDA product code for PERLINK SCREEN, KIRAN SCREEN?

The FDA product code for PERLINK SCREEN, KIRAN SCREEN is EAM.

Related Clinical Trials

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Other records listing Perlink USA, 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.

K922358STERLING POWDER FREE PATIENT EXAMINATION GLOVESK924959STERLING LATEX EXAM GLOVE, HYPO-ALLERGENICK921438DISPOSABLE LATEX EXAMINATION GLOVESK901790THERMOMETER, MERCURY/CLINICALK896708PERLINK CASSETTE, KIRAN CASSETTE

Related Devices (Code: EAM)

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.

K974423ULTRA-VISION MAMMOGRAPHY DETAIL, ULTRA-VISION MAMMOGRAPHY FAST DETAILSterling Diagnostic Imaging, Inc.K963913MD100 & MM150Konica Medical Corp.K954161JPI INTENSIFYING SCREENJpi Healthcare Co, Ltd.K943822FUJI UM MAMMO SERIES INTENSIFY SCREENS:Fujifilm Medical System U.S.A., Inc.K943823FUJI FG SERIES INTENSIFYING SCREENS: FG-3-4-8-12Fujifilm Medical System U.S.A., Inc.K943821KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPECFujifilm Medical System U.S.A., Inc.

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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