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FDA 510(k)

STOMA MEASURING DEVICE

K-Number: K914482 · 1991-12-27

ApplicantBiosearch Medical Products, Inc.
Decision Date1991-12-27
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STOMA MEASURING DEVICE 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 1991-12-27 under 510(k) number K914482. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOMA MEASURING DEVICE?

STOMA MEASURING DEVICE is a medical device that received FDA 510(k) clearance on 1991-12-27. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K914482.

When did STOMA MEASURING DEVICE receive FDA 510(k) clearance?

STOMA MEASURING DEVICE received FDA 510(k) clearance on 1991-12-27, under 510(k) number K914482.

Who is the listed applicant for STOMA MEASURING DEVICE?

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 STOMA MEASURING DEVICE?

The FDA product code for STOMA MEASURING DEVICE is FPD.

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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: FPD)

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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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