BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES
K-Number: K931910 · 1993-10-01
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Device Summary
Frequently Asked Questions
What is the BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES?
BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES is a medical device that received FDA 510(k) clearance on 1993-10-01. The listed applicant is Brillenerzeugung Pomberger. The 510(k) number is K931910.
When did BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES receive FDA 510(k) clearance?
BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES received FDA 510(k) clearance on 1993-10-01, under 510(k) number K931910.
Who is the listed applicant for BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES?
The FDA 510(k) record lists Brillenerzeugung Pomberger as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES?
The FDA product code for BRILLENERZEUGUNG POMBERGER OR MULTIPLE SUNGLASSES is HQY.
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 Brillenerzeugung Pomberger 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: HQY)
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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