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FDA 510(k)

6 FRENCH CATHETER

K-Number: K922564 · 1992-12-17

ApplicantS. and H. Engineering, Inc.
Decision Date1992-12-17
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

6 FRENCH CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is S. and H. Engineering, Inc.. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K922564. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 6 FRENCH CATHETER?

6 FRENCH CATHETER is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is S. and H. Engineering, Inc.. The 510(k) number is K922564.

When did 6 FRENCH CATHETER receive FDA 510(k) clearance?

6 FRENCH CATHETER received FDA 510(k) clearance on 1992-12-17, under 510(k) number K922564.

Who is the listed applicant for 6 FRENCH CATHETER?

The FDA 510(k) record lists S. and H. Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 6 FRENCH CATHETER?

The FDA product code for 6 FRENCH CATHETER is JAQ.

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Other records listing S. and H. Engineering, 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.

K962487BREAST TREATMENT AID M200K961467HEAD RETAINING DEVICEK961170BREAST TREATMENT AID

Related Devices (Code: JAQ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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