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FDA 510(k)

DOBBHOFF FEEDING TUBE W/HYDROMER LUB

K-Number: K831868 · 1983-07-12

Decision Date1983-07-12
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DOBBHOFF FEEDING TUBE W/HYDROMER LUB is the device name listed in this FDA 510(k) record. The listed applicant is Biosearch Medical Products, Inc.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831868. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOBBHOFF FEEDING TUBE W/HYDROMER LUB?

DOBBHOFF FEEDING TUBE W/HYDROMER LUB is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K831868.

When did DOBBHOFF FEEDING TUBE W/HYDROMER LUB receive FDA 510(k) clearance?

DOBBHOFF FEEDING TUBE W/HYDROMER LUB received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831868.

Who is the listed applicant for DOBBHOFF FEEDING TUBE W/HYDROMER LUB?

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

What is the FDA product code for DOBBHOFF FEEDING TUBE W/HYDROMER LUB?

The FDA product code for DOBBHOFF FEEDING TUBE W/HYDROMER LUB is KNT.

Related Clinical Trials

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.

Other records listing Biosearch Medical Products, Inc. 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.

View all 70 devices →

Related Devices (Code: KNT)

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.

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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