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FDA 510(k)

COUNTER, SPONGE

K-Number: K770698 · 1977-05-06

ApplicantDevon Industries, Inc.
Decision Date1977-05-06
Product Code
DecisionSubstantially Equivalent

Device Summary

COUNTER, SPONGE 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 1977-05-06 under 510(k) number K770698. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COUNTER, SPONGE?

COUNTER, SPONGE is a medical device that received FDA 510(k) clearance on 1977-05-06. The listed applicant is Devon Industries, Inc.. The 510(k) number is K770698.

When did COUNTER, SPONGE receive FDA 510(k) clearance?

COUNTER, SPONGE received FDA 510(k) clearance on 1977-05-06, under 510(k) number K770698.

Who is the listed applicant for COUNTER, SPONGE?

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 DEVICEK943892POINT OF USE SHARPS A GATORK944114PHLEBOTOMY UNIT SHARPS A GATORK945197THE SHARPS COLLECTION AND DISPOSAL SYSTEM

View all 47 devices →

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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