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FDA 510(k)

BIOSEARCH 3600 ENTRI FEEDING PUMP

K-Number: K883587 · 1988-11-08

ApplicantBiosearch Medical Products, Inc.
Decision Date1988-11-08
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BIOSEARCH 3600 ENTRI FEEDING PUMP 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 1988-11-08 under 510(k) number K883587. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOSEARCH 3600 ENTRI FEEDING PUMP?

BIOSEARCH 3600 ENTRI FEEDING PUMP is a medical device that received FDA 510(k) clearance on 1988-11-08. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K883587.

When did BIOSEARCH 3600 ENTRI FEEDING PUMP receive FDA 510(k) clearance?

BIOSEARCH 3600 ENTRI FEEDING PUMP received FDA 510(k) clearance on 1988-11-08, under 510(k) number K883587.

Who is the listed applicant for BIOSEARCH 3600 ENTRI FEEDING PUMP?

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 BIOSEARCH 3600 ENTRI FEEDING PUMP?

The FDA product code for BIOSEARCH 3600 ENTRI FEEDING PUMP is FRN.

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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.

K051480ENTERAL FEEDING TUBEK970145PERINEOMETER & VAGINAL PROBE (BIOFEEDBACK MONITOR #20 AND VAGINAL PROBE)K964871BIOSEARCH SYRING FLUSHING/CLEANING PUMP FOR BIOSEARCH ENDOSCOPIC INSTRUMENTSK951260URINARY INTERMITTENT CATHETERS W/O HYDROMER HYDROPHILIC LUBRICANTK944614MEGA-BRUSH, ENDOSCOPIC MASS CYTOLOGY - CELLUAR RETRIEVAL SYSTEMK932295NON-BALLOON REPLACEMENT GASTROSTOMY KIT

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Related Devices (Code: FRN)

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.

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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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