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FDA 510(k)

STICK-GARD STERILE CAP

K-Number: K902682 · 1990-09-26

ApplicantIntegrated Medical Systems, Inc.
Decision Date1990-09-26
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STICK-GARD STERILE CAP is the device name listed in this FDA 510(k) record. The listed applicant is Integrated Medical Systems, Inc.. It received FDA 510(k) clearance on 1990-09-26 under 510(k) number K902682. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STICK-GARD STERILE CAP?

STICK-GARD STERILE CAP is a medical device that received FDA 510(k) clearance on 1990-09-26. The listed applicant is Integrated Medical Systems, Inc.. The 510(k) number is K902682.

When did STICK-GARD STERILE CAP receive FDA 510(k) clearance?

STICK-GARD STERILE CAP received FDA 510(k) clearance on 1990-09-26, under 510(k) number K902682.

Who is the listed applicant for STICK-GARD STERILE CAP?

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

What is the FDA product code for STICK-GARD STERILE CAP?

The FDA product code for STICK-GARD STERILE CAP is LDQ.

Related Clinical Trials

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Other records listing Integrated Medical Systems, 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.

K082256LIFE SUPPORT FOR TRAUMA AND TRNSPORT (LSTAT) G6 LITEK895414MULTIMED (TM) PULMONARY FUNCTION TESTING SYSTEMK871659IMS-2000S STRESS MONITORK870934IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM

Related Devices (Code: LDQ)

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.

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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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