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FDA 510(k)

DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST

K-Number: K913736 · 1992-02-07

Decision Date1992-02-07
Product CodeFAP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST 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 1992-02-07 under 510(k) number K913736. The device is classified under product code FAP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST?

DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K913736.

When did DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST receive FDA 510(k) clearance?

DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST received FDA 510(k) clearance on 1992-02-07, under 510(k) number K913736.

Who is the listed applicant for DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST?

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 ANORECT BIOFEED SYST FIVE DIV FECAL CONST?

The FDA product code for DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST is FAP.

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: FAP)

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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