FDA 510(k)

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider

K-번호: K162751 · 2017-05-01

신청자Surgical Instrument Services and Savings, Inc.

결정일2017-05-01

제품 코드NUJ

자문 위원회SU

결정Substantially Equivalent

기기 요약

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instrument Services and Savings, Inc.. It received FDA 510(k) clearance on 2017-05-01 under 510(k) number K162751. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is a medical device that received FDA 510(k) clearance on 2017-05-01. The listed applicant is Surgical Instrument Services and Savings, Inc.. The 510(k) number is K162751.

When did Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider receive FDA 510(k) clearance?

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider received FDA 510(k) clearance on 2017-05-01, under 510(k) number K162751.

Who is the listed applicant for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?

The FDA 510(k) record lists Surgical Instrument Services and Savings, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?

The FDA product code for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is NUJ.

Surgical Instrument Services and Savings, Inc.를 신청인으로 등재한 기타 기록

K232130Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheter K152313Medline ReNewal Reprocessed Endopath Endoscopic Instruments

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