Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CAPD SAFE LOCK TRANSFER SET

K-Number: K822543 · 1982-10-13

Decision Date1982-10-13
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CAPD SAFE LOCK TRANSFER SET 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 K822543. 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 CAPD SAFE LOCK TRANSFER SET?

CAPD SAFE LOCK TRANSFER SET 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 K822543.

When did CAPD SAFE LOCK TRANSFER SET receive FDA 510(k) clearance?

CAPD SAFE LOCK TRANSFER SET received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822543.

Who is the listed applicant for CAPD SAFE LOCK TRANSFER SET?

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 CAPD SAFE LOCK TRANSFER SET?

The FDA product code for CAPD SAFE LOCK TRANSFER SET is FKX.

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 American Medical Products, 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 30 devices →

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.

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.

↑