STORZ DP4600 ANTERIOR INTRAOCULAR PRESSURE CONTROL PACK
K-Number: K961820 · 1996-07-25
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Device Summary
Frequently Asked Questions
What is the STORZ DP4600 ANTERIOR INTRAOCULAR PRESSURE CONTROL PACK?
STORZ DP4600 ANTERIOR INTRAOCULAR PRESSURE CONTROL PACK is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Storz Instrument Co.. The 510(k) number is K961820.
When did STORZ DP4600 ANTERIOR INTRAOCULAR PRESSURE CONTROL PACK receive FDA 510(k) clearance?
STORZ DP4600 ANTERIOR INTRAOCULAR PRESSURE CONTROL PACK received FDA 510(k) clearance on 1996-07-25, under 510(k) number K961820.
Who is the listed applicant for STORZ DP4600 ANTERIOR INTRAOCULAR PRESSURE CONTROL PACK?
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 STORZ DP4600 ANTERIOR INTRAOCULAR PRESSURE CONTROL PACK?
The FDA product code for STORZ DP4600 ANTERIOR INTRAOCULAR PRESSURE CONTROL PACK is HQC.
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: HQC)
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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