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FDA 510(k)

SMALL BOWEL ANALYSIS SOFTWARE

K-Number: K942247 · 1996-04-09

ApplicantSandhill Scientific, Inc.
Decision Date1996-04-09
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SMALL BOWEL ANALYSIS SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Sandhill Scientific, Inc.. It received FDA 510(k) clearance on 1996-04-09 under 510(k) number K942247. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMALL BOWEL ANALYSIS SOFTWARE?

SMALL BOWEL ANALYSIS SOFTWARE is a medical device that received FDA 510(k) clearance on 1996-04-09. The listed applicant is Sandhill Scientific, Inc.. The 510(k) number is K942247.

When did SMALL BOWEL ANALYSIS SOFTWARE receive FDA 510(k) clearance?

SMALL BOWEL ANALYSIS SOFTWARE received FDA 510(k) clearance on 1996-04-09, under 510(k) number K942247.

Who is the listed applicant for SMALL BOWEL ANALYSIS SOFTWARE?

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

What is the FDA product code for SMALL BOWEL ANALYSIS SOFTWARE?

The FDA product code for SMALL BOWEL ANALYSIS SOFTWARE is FFX.

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Other records listing Sandhill Scientific, 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.

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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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