VERIFY 275F GRAVITY INDICATORS
K-Number: K083643 · 2009-08-07
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Device Summary
Frequently Asked Questions
What is the VERIFY 275F GRAVITY INDICATORS?
VERIFY 275F GRAVITY INDICATORS is a medical device that received FDA 510(k) clearance on 2009-08-07. The listed applicant is STERIS Corporation. The 510(k) number is K083643.
When did VERIFY 275F GRAVITY INDICATORS receive FDA 510(k) clearance?
VERIFY 275F GRAVITY INDICATORS received FDA 510(k) clearance on 2009-08-07, under 510(k) number K083643.
Who is the listed applicant for VERIFY 275F GRAVITY INDICATORS?
The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERIFY 275F GRAVITY INDICATORS?
The FDA product code for VERIFY 275F GRAVITY INDICATORS is JOJ.
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 STERIS Corporation 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: JOJ)
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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