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FDA 510(k)

ANALGRAPH

K-Number: K941801 · 1995-09-08

ApplicantSandhill Scientific, Inc.
Decision Date1995-09-08
Product CodeKLA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANALGRAPH 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 1995-09-08 under 510(k) number K941801. The device is classified under product code KLA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALGRAPH?

ANALGRAPH is a medical device that received FDA 510(k) clearance on 1995-09-08. The listed applicant is Sandhill Scientific, Inc.. The 510(k) number is K941801.

When did ANALGRAPH receive FDA 510(k) clearance?

ANALGRAPH received FDA 510(k) clearance on 1995-09-08, under 510(k) number K941801.

Who is the listed applicant for ANALGRAPH?

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 ANALGRAPH?

The FDA product code for ANALGRAPH is KLA.

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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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Related Devices (Code: KLA)

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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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