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FDA 510(k)

SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER

K-Number: K882881 · 1988-07-28

ApplicantSakura Finetek U.S.A., Inc.
Decision Date1988-07-28
Product CodeKES
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER is the device name listed in this FDA 510(k) record. The listed applicant is Sakura Finetek U.S.A., Inc.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K882881. The device is classified under product code KES. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER?

SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Sakura Finetek U.S.A., Inc.. The 510(k) number is K882881.

When did SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER receive FDA 510(k) clearance?

SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882881.

Who is the listed applicant for SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER?

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

What is the FDA product code for SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER?

The FDA product code for SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER is KES.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Sakura Finetek U.S.A., 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.

K893811SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEMK881165SAKURA HEM-480 ELECTRON MICROSCOPY PROCESSORK874897SAKURA DRS-60 AUTOMATIC SLIDE STAINER

Related Devices (Code: KES)

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.

K872874MICROSCOPE COVER GLASSESAbco Dealers, Inc.K771925KRYSTALONR LIQ. MOUNTING MED.&COVERSLIPHarleco

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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