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FDA 510(k)

DIGITAL MANOMETER (DM 50)

K-Number: K901998 · 1990-07-25

Decision Date1990-07-25
Product CodeBXR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DIGITAL MANOMETER (DM 50) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Support Products, Inc.. It received FDA 510(k) clearance on 1990-07-25 under 510(k) number K901998. The device is classified under product code BXR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL MANOMETER (DM 50)?

DIGITAL MANOMETER (DM 50) is a medical device that received FDA 510(k) clearance on 1990-07-25. The listed applicant is Medical Support Products, Inc.. The 510(k) number is K901998.

When did DIGITAL MANOMETER (DM 50) receive FDA 510(k) clearance?

DIGITAL MANOMETER (DM 50) received FDA 510(k) clearance on 1990-07-25, under 510(k) number K901998.

Who is the listed applicant for DIGITAL MANOMETER (DM 50)?

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

What is the FDA product code for DIGITAL MANOMETER (DM 50)?

The FDA product code for DIGITAL MANOMETER (DM 50) is BXR.

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.

Related Devices (Code: BXR)

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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