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FDA 510(k)

NASAL GASTRIC TUBE RETAINER

K-Number: K780396 · 1978-03-22

ApplicantMor-Mac, Inc.
Decision Date1978-03-22
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NASAL GASTRIC TUBE RETAINER is the device name listed in this FDA 510(k) record. The listed applicant is Mor-Mac, Inc.. It received FDA 510(k) clearance on 1978-03-22 under 510(k) number K780396. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NASAL GASTRIC TUBE RETAINER?

NASAL GASTRIC TUBE RETAINER is a medical device that received FDA 510(k) clearance on 1978-03-22. The listed applicant is Mor-Mac, Inc.. The 510(k) number is K780396.

When did NASAL GASTRIC TUBE RETAINER receive FDA 510(k) clearance?

NASAL GASTRIC TUBE RETAINER received FDA 510(k) clearance on 1978-03-22, under 510(k) number K780396.

Who is the listed applicant for NASAL GASTRIC TUBE RETAINER?

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

What is the FDA product code for NASAL GASTRIC TUBE RETAINER?

The FDA product code for NASAL GASTRIC TUBE RETAINER is FPK.

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Related Devices (Code: FPK)

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.

K131517MEDRAD TWIST & GO HIGH PRESSURE CONNECTOR TUBINGMedrad, Inc. / Bayer Medical Care, Inc.K063114DISPOSABLE TRANSFER SETS WITH AND WITHOUT SWABBABLE VALVES AND/OR CHECK VALVESCoeur, Inc.K063239LIFESHIELD LATEX-FREE GRAVITECH FLOW CONTROLLER I.V. SETS, MODELS 17528, 17527, 17525 & 17526Hospira, Inc.K052431MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1Medtronic MinimedK041178EMPOWER TRANSFER SET, (CAT. NO. 7725)E-Z-Em, Inc.K031808MEDRAD SWABBABLE VALVE TRANSFER SETMedrad, Inc.

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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