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FDA 510(k)

N. M. BEALE COMPANY VU-THRU WATER BOTTLE

K-Number: K903834 · 1990-09-24

Decision Date1990-09-24
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

N. M. BEALE COMPANY VU-THRU WATER BOTTLE is the device name listed in this FDA 510(k) record. The listed applicant is N.M. Beale Co., Inc.. It received FDA 510(k) clearance on 1990-09-24 under 510(k) number K903834. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N. M. BEALE COMPANY VU-THRU WATER BOTTLE?

N. M. BEALE COMPANY VU-THRU WATER BOTTLE is a medical device that received FDA 510(k) clearance on 1990-09-24. The listed applicant is N.M. Beale Co., Inc.. The 510(k) number is K903834.

When did N. M. BEALE COMPANY VU-THRU WATER BOTTLE receive FDA 510(k) clearance?

N. M. BEALE COMPANY VU-THRU WATER BOTTLE received FDA 510(k) clearance on 1990-09-24, under 510(k) number K903834.

Who is the listed applicant for N. M. BEALE COMPANY VU-THRU WATER BOTTLE?

The FDA 510(k) record lists N.M. Beale Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for N. M. BEALE COMPANY VU-THRU WATER BOTTLE?

The FDA product code for N. M. BEALE COMPANY VU-THRU WATER BOTTLE is OCX.

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 N.M. Beale Co., 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.

Related Devices (Code: OCX)

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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