PIGGY LOCK NEEDLE HOUSING
K-Number: K910546 · 1991-04-29
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Device Summary
Frequently Asked Questions
What is the PIGGY LOCK NEEDLE HOUSING?
PIGGY LOCK NEEDLE HOUSING is a medical device that received FDA 510(k) clearance on 1991-04-29. The listed applicant is Icu Medical, Inc.. The 510(k) number is K910546.
When did PIGGY LOCK NEEDLE HOUSING receive FDA 510(k) clearance?
PIGGY LOCK NEEDLE HOUSING received FDA 510(k) clearance on 1991-04-29, under 510(k) number K910546.
Who is the listed applicant for PIGGY LOCK NEEDLE HOUSING?
The FDA 510(k) record lists Icu Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PIGGY LOCK NEEDLE HOUSING?
The FDA product code for PIGGY LOCK NEEDLE HOUSING is FPA.
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 Icu Medical, 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.
Related Devices (Code: FPA)
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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