FRAME, SPECTACLES
K-Number: K945350 · 1994-12-13
Advertisement
Device Summary
Frequently Asked Questions
What is the FRAME, SPECTACLES?
FRAME, SPECTACLES is a medical device that received FDA 510(k) clearance on 1994-12-13. The listed applicant is Taiwan Eva Industrial Co., Inc.. The 510(k) number is K945350.
When did FRAME, SPECTACLES receive FDA 510(k) clearance?
FRAME, SPECTACLES received FDA 510(k) clearance on 1994-12-13, under 510(k) number K945350.
Who is the listed applicant for FRAME, SPECTACLES?
The FDA 510(k) record lists Taiwan Eva Industrial Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FRAME, SPECTACLES?
The FDA product code for FRAME, SPECTACLES is HQZ.
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 Taiwan Eva Industrial 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: HQZ)
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.
Advertisement