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FDA 510(k)

SALTER LABS DISPOSABLE NIPPLE AND NUT

K-Number: K912174 · 1991-07-24

ApplicantSalter Labs
Decision Date1991-07-24
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SALTER LABS DISPOSABLE NIPPLE AND NUT is the device name listed in this FDA 510(k) record. The listed applicant is Salter Labs. It received FDA 510(k) clearance on 1991-07-24 under 510(k) number K912174. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALTER LABS DISPOSABLE NIPPLE AND NUT?

SALTER LABS DISPOSABLE NIPPLE AND NUT is a medical device that received FDA 510(k) clearance on 1991-07-24. The listed applicant is Salter Labs. The 510(k) number is K912174.

When did SALTER LABS DISPOSABLE NIPPLE AND NUT receive FDA 510(k) clearance?

SALTER LABS DISPOSABLE NIPPLE AND NUT received FDA 510(k) clearance on 1991-07-24, under 510(k) number K912174.

Who is the listed applicant for SALTER LABS DISPOSABLE NIPPLE AND NUT?

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

What is the FDA product code for SALTER LABS DISPOSABLE NIPPLE AND NUT?

The FDA product code for SALTER LABS DISPOSABLE NIPPLE AND NUT is CAN.

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Related Devices (Code: CAN)

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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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