Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695

K-Number: K870278 · 1987-02-20

Decision Date1987-02-20
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695 is the device name listed in this FDA 510(k) record. The listed applicant is Ryder Intl. Corp.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K870278. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 10 devices →

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.

↑