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FDA 510(k)

BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005

K-Number: K954278 · 1995-10-02

ApplicantBeta Medical Products, Inc.
Decision Date1995-10-02
Product CodeMMZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005 is the device name listed in this FDA 510(k) record. The listed applicant is Beta Medical Products, Inc.. It received FDA 510(k) clearance on 1995-10-02 under 510(k) number K954278. The device is classified under product code MMZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005?

BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005 is a medical device that received FDA 510(k) clearance on 1995-10-02. The listed applicant is Beta Medical Products, Inc.. The 510(k) number is K954278.

When did BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005 receive FDA 510(k) clearance?

BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005 received FDA 510(k) clearance on 1995-10-02, under 510(k) number K954278.

Who is the listed applicant for BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005?

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

What is the FDA product code for BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005?

The FDA product code for BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005 is MMZ.

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Related Devices (Code: MMZ)

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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