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FDA 510(k)

BOBES SLIT LAMP

K-Number: K945445 · 1995-10-17

ApplicantBobes S.A.
Decision Date1995-10-17
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BOBES SLIT LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Bobes S.A.. It received FDA 510(k) clearance on 1995-10-17 under 510(k) number K945445. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOBES SLIT LAMP?

BOBES SLIT LAMP is a medical device that received FDA 510(k) clearance on 1995-10-17. The listed applicant is Bobes S.A.. The 510(k) number is K945445.

When did BOBES SLIT LAMP receive FDA 510(k) clearance?

BOBES SLIT LAMP received FDA 510(k) clearance on 1995-10-17, under 510(k) number K945445.

Who is the listed applicant for BOBES SLIT LAMP?

The FDA 510(k) record lists Bobes S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOBES SLIT LAMP?

The FDA product code for BOBES SLIT LAMP is HJO.

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 Bobes S.A. 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: HJO)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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