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FDA 510(k)

INJECT-EASE

K-Number: K872233 · 1987-09-04

ApplicantPalco Laboratories, Inc.
Decision Date1987-09-04
Product CodeKZH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INJECT-EASE is the device name listed in this FDA 510(k) record. The listed applicant is Palco Laboratories, Inc.. It received FDA 510(k) clearance on 1987-09-04 under 510(k) number K872233. The device is classified under product code KZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECT-EASE?

INJECT-EASE is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is Palco Laboratories, Inc.. The 510(k) number is K872233.

When did INJECT-EASE receive FDA 510(k) clearance?

INJECT-EASE received FDA 510(k) clearance on 1987-09-04, under 510(k) number K872233.

Who is the listed applicant for INJECT-EASE?

The FDA 510(k) record lists Palco Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INJECT-EASE?

The FDA product code for INJECT-EASE is KZH.

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Other records listing Palco Laboratories, 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.

K942810PALCO LABS COLD POUCHK943842PULSE OXIMETER MODEL 305K920066PALCO LABS MODEL 340 PULSE OXIMETERK913694PALCO LABS LOADMATICK911191PALCO LABS MODEL 300 OXYGEN/PULSE MONITORK904988PALCO LABS MODEL 400 OXYGEN/PULSE MONITOR

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Related Devices (Code: KZH)

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.

K243232GripMateSynthon Hispania S.L.K213429AccuSert Needle InserterEmed Technologies CorporationK163400Orbit InserterYpsomed AGK160860MiniMed Quick-serterMedtronic MinimedK124026LOBSTER AUTO-INJECTORScandinavian Health LimitedK122837AUTOJECT 2 FOR GLASSY SYRINGEOwen Mumford, Ltd.

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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