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FDA 510(k)

ARROW PERITONEAL LAVAGE CATHERIZATION K

K-Number: K811627 · 1981-08-10

ApplicantArrow Intl., Inc.
Decision Date1981-08-10
Product CodeGBW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARROW PERITONEAL LAVAGE CATHERIZATION K is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1981-08-10 under 510(k) number K811627. The device is classified under product code GBW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW PERITONEAL LAVAGE CATHERIZATION K?

ARROW PERITONEAL LAVAGE CATHERIZATION K is a medical device that received FDA 510(k) clearance on 1981-08-10. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K811627.

When did ARROW PERITONEAL LAVAGE CATHERIZATION K receive FDA 510(k) clearance?

ARROW PERITONEAL LAVAGE CATHERIZATION K received FDA 510(k) clearance on 1981-08-10, under 510(k) number K811627.

Who is the listed applicant for ARROW PERITONEAL LAVAGE CATHERIZATION K?

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

What is the FDA product code for ARROW PERITONEAL LAVAGE CATHERIZATION K?

The FDA product code for ARROW PERITONEAL LAVAGE CATHERIZATION K is GBW.

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Other records listing Arrow Intl., Inc. as applicant

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Related Devices (Code: GBW)

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.

K992907INTRADUCERTaut, Inc.K992904MINI-PORTTaut, Inc.K972112INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450Taut, Inc.K961194ANTIMICROBIAL MEDIASTINAL SILICONE DRAINSil-Med Corp.K960426MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETERMedical Components, Inc.K942709MEDIASTINAL SILICONE DRAINSSil-Med Corp.

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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