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FDA 510(k)

MODIFIED SURGICAL STARTER KIT

K-Number: K862961 · 1986-08-20

ApplicantDevon Industries, Inc.
Decision Date1986-08-20
Product Code
DecisionSubstantially Equivalent

Device Summary

MODIFIED SURGICAL STARTER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1986-08-20 under 510(k) number K862961. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SURGICAL STARTER KIT?

MODIFIED SURGICAL STARTER KIT is a medical device that received FDA 510(k) clearance on 1986-08-20. The listed applicant is Devon Industries, Inc.. The 510(k) number is K862961.

When did MODIFIED SURGICAL STARTER KIT receive FDA 510(k) clearance?

MODIFIED SURGICAL STARTER KIT received FDA 510(k) clearance on 1986-08-20, under 510(k) number K862961.

Who is the listed applicant for MODIFIED SURGICAL STARTER KIT?

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

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Other records listing Devon Industries, 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.

K961993BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)K954015ABG POINT LOK NEEDLE PROTECTION DEVICEK946289DEVONS POINT LOK NEEDLE PROTECTION DEVICEK945197THE SHARPS COLLECTION AND DISPOSAL SYSTEMK944114PHLEBOTOMY UNIT SHARPS A GATORK943892POINT OF USE SHARPS A GATOR

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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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