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FDA 510(k)

CANNUOATED TROCHAR

K-Number: K820776 · 1982-04-15

ApplicantThe Anspach Effort, Inc.
Decision Date1982-04-15
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CANNUOATED TROCHAR is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 1982-04-15 under 510(k) number K820776. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNUOATED TROCHAR?

CANNUOATED TROCHAR is a medical device that received FDA 510(k) clearance on 1982-04-15. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K820776.

When did CANNUOATED TROCHAR receive FDA 510(k) clearance?

CANNUOATED TROCHAR received FDA 510(k) clearance on 1982-04-15, under 510(k) number K820776.

Who is the listed applicant for CANNUOATED TROCHAR?

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

What is the FDA product code for CANNUOATED TROCHAR?

The FDA product code for CANNUOATED TROCHAR is HRX.

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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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