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FDA 510(k)

PERFORATED SOAKING TUBE

K-Number: K874596 · 1987-12-02

Decision Date1987-12-02
Product CodeGBQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PERFORATED SOAKING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Specialty Medical Products Co.. It received FDA 510(k) clearance on 1987-12-02 under 510(k) number K874596. The device is classified under product code GBQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERFORATED SOAKING TUBE?

PERFORATED SOAKING TUBE is a medical device that received FDA 510(k) clearance on 1987-12-02. The listed applicant is Specialty Medical Products Co.. The 510(k) number is K874596.

When did PERFORATED SOAKING TUBE receive FDA 510(k) clearance?

PERFORATED SOAKING TUBE received FDA 510(k) clearance on 1987-12-02, under 510(k) number K874596.

Who is the listed applicant for PERFORATED SOAKING TUBE?

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

What is the FDA product code for PERFORATED SOAKING TUBE?

The FDA product code for PERFORATED SOAKING TUBE is GBQ.

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 Specialty Medical Products Co. 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: GBQ)

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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