PHOTOSTRESS RECOVERY TESTER
K-Number: K933814 · 1993-12-08
Advertisement
Device Summary
Frequently Asked Questions
What is the PHOTOSTRESS RECOVERY TESTER?
PHOTOSTRESS RECOVERY TESTER is a medical device that received FDA 510(k) clearance on 1993-12-08. The listed applicant is Storz Instrument Co.. The 510(k) number is K933814.
When did PHOTOSTRESS RECOVERY TESTER receive FDA 510(k) clearance?
PHOTOSTRESS RECOVERY TESTER received FDA 510(k) clearance on 1993-12-08, under 510(k) number K933814.
Who is the listed applicant for PHOTOSTRESS RECOVERY TESTER?
The FDA 510(k) record lists Storz Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHOTOSTRESS RECOVERY TESTER?
The FDA product code for PHOTOSTRESS RECOVERY TESTER is GXY.
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 Storz Instrument Co. 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: GXY)
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