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FDA 510(k)

SALMAN SINUS BUTTON

K-Number: K922902 · 1993-05-18

Decision Date1993-05-18
Product CodeKAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SALMAN SINUS BUTTON is the device name listed in this FDA 510(k) record. The listed applicant is Boston Medical Products, Inc.. It received FDA 510(k) clearance on 1993-05-18 under 510(k) number K922902. The device is classified under product code KAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALMAN SINUS BUTTON?

SALMAN SINUS BUTTON is a medical device that received FDA 510(k) clearance on 1993-05-18. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K922902.

When did SALMAN SINUS BUTTON receive FDA 510(k) clearance?

SALMAN SINUS BUTTON received FDA 510(k) clearance on 1993-05-18, under 510(k) number K922902.

Who is the listed applicant for SALMAN SINUS BUTTON?

The FDA 510(k) record lists Boston Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SALMAN SINUS BUTTON?

The FDA product code for SALMAN SINUS BUTTON is KAM.

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 Boston Medical Products, Inc. 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.

View all 33 devices →

Related Devices (Code: KAM)

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

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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