SNAP-N-PEEL INTRODUCERS
K-Number: K981611 · 1998-07-30
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Device Summary
Frequently Asked Questions
What is the SNAP-N-PEEL INTRODUCERS?
SNAP-N-PEEL INTRODUCERS is a medical device that received FDA 510(k) clearance on 1998-07-30. The listed applicant is Circon Corp.. The 510(k) number is K981611.
When did SNAP-N-PEEL INTRODUCERS receive FDA 510(k) clearance?
SNAP-N-PEEL INTRODUCERS received FDA 510(k) clearance on 1998-07-30, under 510(k) number K981611.
Who is the listed applicant for SNAP-N-PEEL INTRODUCERS?
The FDA 510(k) record lists Circon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SNAP-N-PEEL INTRODUCERS?
The FDA product code for SNAP-N-PEEL INTRODUCERS is KNY.
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 Circon Corp. 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: KNY)
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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