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FDA 510(k)

SUMP DRAIN, W/FILTER, ARGYLE EDLICH

K-Number: K770442 · 1977-03-30

ApplicantSherwood Medical Industries
Decision Date1977-03-30
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUMP DRAIN, W/FILTER, ARGYLE EDLICH is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1977-03-30 under 510(k) number K770442. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUMP DRAIN, W/FILTER, ARGYLE EDLICH?

SUMP DRAIN, W/FILTER, ARGYLE EDLICH is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is Sherwood Medical Industries. The 510(k) number is K770442.

When did SUMP DRAIN, W/FILTER, ARGYLE EDLICH receive FDA 510(k) clearance?

SUMP DRAIN, W/FILTER, ARGYLE EDLICH received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770442.

Who is the listed applicant for SUMP DRAIN, W/FILTER, ARGYLE EDLICH?

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

What is the FDA product code for SUMP DRAIN, W/FILTER, ARGYLE EDLICH?

The FDA product code for SUMP DRAIN, W/FILTER, ARGYLE EDLICH is GBX.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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Related Devices (Code: GBX)

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.

K082725GRAFTGUARD PRESSURE CONTROLLING SYRINGEMaquet Cardiovascular, LLCK052286DEUTSCH ANTI-BLOCKAGE WOUND DRAINThe Catheter Exchange, Inc.K043515GRAFTSAVERVescare, Inc.K013417MISONIX IRRIGATION SYSTEM MOEDL BC20PMisonix, Inc.K000704DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)Dmc Medical, Ltd.K974233LYSONIX IRRIGATION SYSTEMLysonix, 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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