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FDA 510(k)

SANDHILL ELECTRONIC CALIPER

K-Number: K854933 · 1986-02-12

ApplicantSandhill
Decision Date1986-02-12
Product CodeIXC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SANDHILL ELECTRONIC CALIPER is the device name listed in this FDA 510(k) record. The listed applicant is Sandhill. It received FDA 510(k) clearance on 1986-02-12 under 510(k) number K854933. The device is classified under product code IXC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SANDHILL ELECTRONIC CALIPER?

SANDHILL ELECTRONIC CALIPER is a medical device that received FDA 510(k) clearance on 1986-02-12. The listed applicant is Sandhill. The 510(k) number is K854933.

When did SANDHILL ELECTRONIC CALIPER receive FDA 510(k) clearance?

SANDHILL ELECTRONIC CALIPER received FDA 510(k) clearance on 1986-02-12, under 510(k) number K854933.

Who is the listed applicant for SANDHILL ELECTRONIC CALIPER?

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

What is the FDA product code for SANDHILL ELECTRONIC CALIPER?

The FDA product code for SANDHILL ELECTRONIC CALIPER is IXC.

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.

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Other records listing Sandhill 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.

K863312SANDHILL AMSK821588SANDHILL DMS

Related Devices (Code: IXC)

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.

K991302SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUSSmartlight, Inc.K973965SMART MOTORIZED VIEWERSmartlight, Ltd.K973115ARRIPRO 35 ST/TVArnold & Richter Cine TechnikK970240DIFFUSER PANELFocused Viewer, Inc.K954998LILY DARK VIEWERLily Imaging Solutions Co.K954199VOXBOXVoxel

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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