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FDA 510(k)

POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER

K-Number: K982385 · 1999-02-01

ApplicantPorous Media Corp.
Decision Date1999-02-01
Product CodeKRJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Porous Media Corp.. It received FDA 510(k) clearance on 1999-02-01 under 510(k) number K982385. The device is classified under product code KRJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER?

POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER is a medical device that received FDA 510(k) clearance on 1999-02-01. The listed applicant is Porous Media Corp.. The 510(k) number is K982385.

When did POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER receive FDA 510(k) clearance?

POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER received FDA 510(k) clearance on 1999-02-01, under 510(k) number K982385.

Who is the listed applicant for POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER?

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

What is the FDA product code for POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER?

The FDA product code for POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER is KRJ.

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Other records listing Porous Media 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.

K062091POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATIONK061426OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47K990276POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTERK982127POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTERK965020POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTERK964979POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER

View all 9 devices →

Related Devices (Code: KRJ)

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.

K990276POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTERPorous Media Corp.K940126AVECOR PRE-BYPASS FILTERAvecor Cardiovascular, Inc.K900672PREBYPASS FILTER, CAT. NO. FPB-5American Omni Medical, Inc.K885154INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEMMedtronic Blood Systems, Inc.K884390INTERSEPT* CRYSTALLOID CARDIOPLEGIA FILTERMedtronic Blood Systems, Inc.K884244INTERSEPT* PREBYPASS FILTERMedtronic Blood Systems, 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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