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FDA 510(k)

SURGICAL STARTER KIT

K-Number: K870744 · 1987-04-10

ApplicantDevon Industries, Inc.
Decision Date1987-04-10
Product Code
DecisionUnknown

Device Summary

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 1987-04-10 under 510(k) number K870744. FDA Decision: Unknown.

Frequently Asked Questions

What is the SURGICAL STARTER KIT?

SURGICAL STARTER KIT is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Devon Industries, Inc.. The 510(k) number is K870744.

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

SURGICAL STARTER KIT received FDA 510(k) clearance on 1987-04-10, under 510(k) number K870744.

Who is the listed applicant for 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 SYSTEMK943892POINT OF USE SHARPS A GATORK944114PHLEBOTOMY UNIT 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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