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FDA 510(k)

BIO-INDUSTRY STIM POCHE(R)

K-Number: K894786 · 1989-09-29

Decision Date1989-09-29
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BIO-INDUSTRY STIM POCHE(R) is the device name listed in this FDA 510(k) record. The listed applicant is The Hader Corp.. It received FDA 510(k) clearance on 1989-09-29 under 510(k) number K894786. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO-INDUSTRY STIM POCHE(R)?

BIO-INDUSTRY STIM POCHE(R) is a medical device that received FDA 510(k) clearance on 1989-09-29. The listed applicant is The Hader Corp.. The 510(k) number is K894786.

When did BIO-INDUSTRY STIM POCHE(R) receive FDA 510(k) clearance?

BIO-INDUSTRY STIM POCHE(R) received FDA 510(k) clearance on 1989-09-29, under 510(k) number K894786.

Who is the listed applicant for BIO-INDUSTRY STIM POCHE(R)?

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

What is the FDA product code for BIO-INDUSTRY STIM POCHE(R)?

The FDA product code for BIO-INDUSTRY STIM POCHE(R) is BXN.

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: BXN)

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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