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FDA 510(k)

HAAG-STREIT SLIT LAMP 900

K-Number: K792083 · 1979-11-16

ApplicantLumenis, Inc.
Decision Date1979-11-16
Product CodeHRM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HAAG-STREIT SLIT LAMP 900 is the device name listed in this FDA 510(k) record. The listed applicant is Lumenis, Inc.. It received FDA 510(k) clearance on 1979-11-16 under 510(k) number K792083. The device is classified under product code HRM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAAG-STREIT SLIT LAMP 900?

HAAG-STREIT SLIT LAMP 900 is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Lumenis, Inc.. The 510(k) number is K792083.

When did HAAG-STREIT SLIT LAMP 900 receive FDA 510(k) clearance?

HAAG-STREIT SLIT LAMP 900 received FDA 510(k) clearance on 1979-11-16, under 510(k) number K792083.

Who is the listed applicant for HAAG-STREIT SLIT LAMP 900?

The FDA 510(k) record lists Lumenis, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAAG-STREIT SLIT LAMP 900?

The FDA product code for HAAG-STREIT SLIT LAMP 900 is HRM.

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 Lumenis, 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.

View all 42 devices →

Related Devices (Code: HRM)

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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