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FDA 510(k)

PIGGY LOCK NEEDLE HOUSING

K-Number: K910546 · 1991-04-29

Decision Date1991-04-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PIGGY LOCK NEEDLE HOUSING is the device name listed in this FDA 510(k) record. The listed applicant is Icu Medical, Inc.. It received FDA 510(k) clearance on 1991-04-29 under 510(k) number K910546. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 65 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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