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FDA 510(k)

SAFE LOCK CATHETER S-3

K-Number: K822548 · 1982-10-13

ApplicantAmerican Medical Products, Inc.
Decision Date1982-10-13
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SAFE LOCK CATHETER S-3 is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Products, Inc.. It received FDA 510(k) clearance on 1982-10-13 under 510(k) number K822548. The device is classified under product code FKX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFE LOCK CATHETER S-3?

SAFE LOCK CATHETER S-3 is a medical device that received FDA 510(k) clearance on 1982-10-13. The listed applicant is American Medical Products, Inc.. The 510(k) number is K822548.

When did SAFE LOCK CATHETER S-3 receive FDA 510(k) clearance?

SAFE LOCK CATHETER S-3 received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822548.

Who is the listed applicant for SAFE LOCK CATHETER S-3?

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

What is the FDA product code for SAFE LOCK CATHETER S-3?

The FDA product code for SAFE LOCK CATHETER S-3 is FKX.

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Other records listing American Medical Products, Inc. as applicant

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Related Devices (Code: FKX)

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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