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FDA 510(k)

LAZARUS-NELSON PERITONEAL LAVAGE TRAY

K-Number: K813336 · 1981-12-18

ApplicantAmerican Pharmaseal Div. Ahsc
Decision Date1981-12-18
Product CodeFKO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAZARUS-NELSON PERITONEAL LAVAGE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1981-12-18 under 510(k) number K813336. The device is classified under product code FKO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAZARUS-NELSON PERITONEAL LAVAGE TRAY?

LAZARUS-NELSON PERITONEAL LAVAGE TRAY is a medical device that received FDA 510(k) clearance on 1981-12-18. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K813336.

When did LAZARUS-NELSON PERITONEAL LAVAGE TRAY receive FDA 510(k) clearance?

LAZARUS-NELSON PERITONEAL LAVAGE TRAY received FDA 510(k) clearance on 1981-12-18, under 510(k) number K813336.

Who is the listed applicant for LAZARUS-NELSON PERITONEAL LAVAGE TRAY?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAZARUS-NELSON PERITONEAL LAVAGE TRAY?

The FDA product code for LAZARUS-NELSON PERITONEAL LAVAGE TRAY is FKO.

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Other records listing American Pharmaseal Div. Ahsc as applicant

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Related Devices (Code: FKO)

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.

K964514CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSISCorpak, Inc.K974570PERITONEAL DIALYSIS CATHETER CONNECTORMedigroup, Inc.K910787TITANIUM CONNECTOR (2 PART)Accurate Surgical Instruments Co.K885037AMUKIN 50% - AIRSPRAY(R)Bernard J. Cooney, P.A.K874650PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM)Quinton, Inc.K872221DIALY-NATE SET & DIALY-NATE CATHETERGesco Intl., Inc.

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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