CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695
K-Number: K870278 · 1987-02-20
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Device Summary
Frequently Asked Questions
What is the CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695?
CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695 is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Ryder Intl. Corp.. The 510(k) number is K870278.
When did CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695 receive FDA 510(k) clearance?
CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695 received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870278.
Who is the listed applicant for CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695?
The FDA 510(k) record lists Ryder Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695?
The FDA product code for CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695 is LPN.
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 Ryder Intl. Corp. 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: LPN)
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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