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FDA 510(k)

BLOOD LINE COMP. NEG. PRESS. PILLOW

K-Number: K772355 · 1978-01-26

ApplicantCordis Corp.
Decision Date1978-01-26
Product CodeFIW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BLOOD LINE COMP. NEG. PRESS. PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1978-01-26 under 510(k) number K772355. The device is classified under product code FIW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD LINE COMP. NEG. PRESS. PILLOW?

BLOOD LINE COMP. NEG. PRESS. PILLOW is a medical device that received FDA 510(k) clearance on 1978-01-26. The listed applicant is Cordis Corp.. The 510(k) number is K772355.

When did BLOOD LINE COMP. NEG. PRESS. PILLOW receive FDA 510(k) clearance?

BLOOD LINE COMP. NEG. PRESS. PILLOW received FDA 510(k) clearance on 1978-01-26, under 510(k) number K772355.

Who is the listed applicant for BLOOD LINE COMP. NEG. PRESS. PILLOW?

The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD LINE COMP. NEG. PRESS. PILLOW?

The FDA product code for BLOOD LINE COMP. NEG. PRESS. PILLOW is FIW.

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Other records listing Cordis Corp. 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.

K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERK101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIREK082143MICRO GUIDE CATHETER XPK062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MBK060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAXK050645CORDIS AMIIA .014 PTA BALLOON CATHETER

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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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