R &D BATTERIES, INC. PART # 5015, 5192, 5482
K-Number: K933513 · 1993-11-24
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Device Summary
Frequently Asked Questions
What is the R &D BATTERIES, INC. PART # 5015, 5192, 5482?
R &D BATTERIES, INC. PART # 5015, 5192, 5482 is a medical device that received FDA 510(k) clearance on 1993-11-24. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K933513.
When did R &D BATTERIES, INC. PART # 5015, 5192, 5482 receive FDA 510(k) clearance?
R &D BATTERIES, INC. PART # 5015, 5192, 5482 received FDA 510(k) clearance on 1993-11-24, under 510(k) number K933513.
Who is the listed applicant for R &D BATTERIES, INC. PART # 5015, 5192, 5482?
The FDA 510(k) record lists R & D Batteries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for R &D BATTERIES, INC. PART # 5015, 5192, 5482?
The FDA product code for R &D BATTERIES, INC. PART # 5015, 5192, 5482 is IYX.
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 R & D Batteries, 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: IYX)
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
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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