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FDA 510(k)

DIGI-SNAP

K-Number: K984169 · 1999-05-26

Decision Date1999-05-26
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DIGI-SNAP is the device name listed in this FDA 510(k) record. The listed applicant is Snap Laboratories, LLC. It received FDA 510(k) clearance on 1999-05-26 under 510(k) number K984169. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGI-SNAP?

DIGI-SNAP is a medical device that received FDA 510(k) clearance on 1999-05-26. The listed applicant is Snap Laboratories, LLC. The 510(k) number is K984169.

When did DIGI-SNAP receive FDA 510(k) clearance?

DIGI-SNAP received FDA 510(k) clearance on 1999-05-26, under 510(k) number K984169.

Who is the listed applicant for DIGI-SNAP?

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

What is the FDA product code for DIGI-SNAP?

The FDA product code for DIGI-SNAP is MNR.

Other records listing Snap Laboratories, LLC 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.

Related Devices (Code: MNR)

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.

Official Source

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