NM INJECTION NEEDLES

Endoscopic Injection Needle, Gastroenterology-urology

OLYMPUS CORP.

The following data is part of a premarket notification filed by Olympus Corp. with the FDA for Nm Injection Needles.

Pre-market Notification Details

• Device ID: K902736
• 510k Number: K902736
• Device Name: NM INJECTION NEEDLES
• Classification: Endoscopic Injection Needle, Gastroenterology-urology
• Applicant: OLYMPUS CORP. 4 NEVADA DR. Lake Success, NY 11042
• Contact: Daniel J Dillon
• Correspondent: Daniel J Dillon; OLYMPUS CORP. 4 NEVADA DR. Lake Success, NY 11042
• Product Code: FBK
• CFR Regulation Number: 876.1500 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1990-06-21
• Decision Date: 1990-08-24

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
14953170260114	K902736	000
14953170259873	K902736	000
14953170259859	K902736	000
14953170259835	K902736	000
14953170259811	K902736	000
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14953170259736	K902736	000
14953170259712	K902736	000
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14953170260091	K902736	000
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14953170260039	K902736	000
14953170260015	K902736	000
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14953170034265	K902736	000
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14953170035019	K902736	000
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14953170034913	K902736	000
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14953170034814	K902736	000
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14953170034661	K902736	000
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14953170381956	K902736	000