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FDA 510(k)

AMCATH COAGULATION PROBE

K-Number: K902555 · 1990-06-20

ApplicantIntl. Medical, Inc.
Decision Date1990-06-20
Product CodeHFG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AMCATH COAGULATION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical, Inc.. It received FDA 510(k) clearance on 1990-06-20 under 510(k) number K902555. The device is classified under product code HFG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMCATH COAGULATION PROBE?

AMCATH COAGULATION PROBE is a medical device that received FDA 510(k) clearance on 1990-06-20. The listed applicant is Intl. Medical, Inc.. The 510(k) number is K902555.

When did AMCATH COAGULATION PROBE receive FDA 510(k) clearance?

AMCATH COAGULATION PROBE received FDA 510(k) clearance on 1990-06-20, under 510(k) number K902555.

Who is the listed applicant for AMCATH COAGULATION PROBE?

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

What is the FDA product code for AMCATH COAGULATION PROBE?

The FDA product code for AMCATH COAGULATION PROBE is HFG.

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Other records listing Intl. 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.

K970507PEAK FLOW METERK943078HOT BIOPSY FORCEPSK940370AMERICAN CATHETER E.R.C.P. CANNULAK940335AMERICAN CATHETER POLY-SNAREK942068AMERICAN CATHETER SPHINCTEROTOMEK930410DURHAM; LUER LOCK EXTENSION SET

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Related Devices (Code: HFG)

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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