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FDA 510(k)

ABSORABLE POLYGLACTIN 910-ANASTOMOTIC

K-Number: K833081 · 1984-01-27

ApplicantETHICON, Inc.
Decision Date1984-01-27
Product Code
DecisionSubstantially Equivalent

Device Summary

ABSORABLE POLYGLACTIN 910-ANASTOMOTIC is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K833081. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABSORABLE POLYGLACTIN 910-ANASTOMOTIC?

ABSORABLE POLYGLACTIN 910-ANASTOMOTIC is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is ETHICON, Inc.. The 510(k) number is K833081.

When did ABSORABLE POLYGLACTIN 910-ANASTOMOTIC receive FDA 510(k) clearance?

ABSORABLE POLYGLACTIN 910-ANASTOMOTIC received FDA 510(k) clearance on 1984-01-27, under 510(k) number K833081.

Who is the listed applicant for ABSORABLE POLYGLACTIN 910-ANASTOMOTIC?

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

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Other records listing ETHICON, 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.

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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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