GRUNDIG ELECTRONICS VARIOUS MODELS
K-Number: K915232 · 1992-01-09
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Device Summary
Frequently Asked Questions
What is the GRUNDIG ELECTRONICS VARIOUS MODELS?
GRUNDIG ELECTRONICS VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Perkins Mfg. Co.. The 510(k) number is K915232.
When did GRUNDIG ELECTRONICS VARIOUS MODELS receive FDA 510(k) clearance?
GRUNDIG ELECTRONICS VARIOUS MODELS received FDA 510(k) clearance on 1992-01-09, under 510(k) number K915232.
Who is the listed applicant for GRUNDIG ELECTRONICS VARIOUS MODELS?
The FDA 510(k) record lists Perkins Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRUNDIG ELECTRONICS VARIOUS MODELS?
The FDA product code for GRUNDIG ELECTRONICS VARIOUS MODELS is IZI.
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 Perkins Mfg. 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: IZI)
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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