DOBBHOFF(R) SINGLE PASS PEG KIT
K-Number: K913784 · 1992-01-15
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Device Summary
Frequently Asked Questions
What is the DOBBHOFF(R) SINGLE PASS PEG KIT?
DOBBHOFF(R) SINGLE PASS PEG KIT is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K913784.
When did DOBBHOFF(R) SINGLE PASS PEG KIT receive FDA 510(k) clearance?
DOBBHOFF(R) SINGLE PASS PEG KIT received FDA 510(k) clearance on 1992-01-15, under 510(k) number K913784.
Who is the listed applicant for DOBBHOFF(R) SINGLE PASS PEG KIT?
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(R) SINGLE PASS PEG KIT?
The FDA product code for DOBBHOFF(R) SINGLE PASS PEG KIT 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.
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
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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