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FDA 510(k)

SNAPDOSE DEVICE

K-Number: K955410 · 1996-05-06

ApplicantAbbott Laboratories
Decision Date1996-05-06
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SNAPDOSE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1996-05-06 under 510(k) number K955410. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNAPDOSE DEVICE?

SNAPDOSE DEVICE is a medical device that received FDA 510(k) clearance on 1996-05-06. The listed applicant is Abbott Laboratories. The 510(k) number is K955410.

When did SNAPDOSE DEVICE receive FDA 510(k) clearance?

SNAPDOSE DEVICE received FDA 510(k) clearance on 1996-05-06, under 510(k) number K955410.

Who is the listed applicant for SNAPDOSE DEVICE?

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

What is the FDA product code for SNAPDOSE DEVICE?

The FDA product code for SNAPDOSE DEVICE is FPA.

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Related Devices (Code: FPA)

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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