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FDA 510(k)

COMFORT PLUS NIPPLE SHIELDS

K-Number: K935340 · 1994-01-21

Decision Date1994-01-21
Product CodeHFS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMFORT PLUS NIPPLE SHIELDS is the device name listed in this FDA 510(k) record. The listed applicant is Marshall Baby Products. It received FDA 510(k) clearance on 1994-01-21 under 510(k) number K935340. The device is classified under product code HFS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMFORT PLUS NIPPLE SHIELDS?

COMFORT PLUS NIPPLE SHIELDS is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Marshall Baby Products. The 510(k) number is K935340.

When did COMFORT PLUS NIPPLE SHIELDS receive FDA 510(k) clearance?

COMFORT PLUS NIPPLE SHIELDS received FDA 510(k) clearance on 1994-01-21, under 510(k) number K935340.

Who is the listed applicant for COMFORT PLUS NIPPLE SHIELDS?

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

What is the FDA product code for COMFORT PLUS NIPPLE SHIELDS?

The FDA product code for COMFORT PLUS NIPPLE SHIELDS is HFS.

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.

Other records listing Marshall Baby Products 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: HFS)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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