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FDA 510(k)

MEDSURG CIRCUMCISION TRAY

K-Number: K920838 · 1993-10-15

ApplicantMedsurg Industries, Inc.
Decision Date1993-10-15
Product CodeHFK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDSURG CIRCUMCISION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1993-10-15 under 510(k) number K920838. The device is classified under product code HFK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSURG CIRCUMCISION TRAY?

MEDSURG CIRCUMCISION TRAY is a medical device that received FDA 510(k) clearance on 1993-10-15. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K920838.

When did MEDSURG CIRCUMCISION TRAY receive FDA 510(k) clearance?

MEDSURG CIRCUMCISION TRAY received FDA 510(k) clearance on 1993-10-15, under 510(k) number K920838.

Who is the listed applicant for MEDSURG CIRCUMCISION TRAY?

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

What is the FDA product code for MEDSURG CIRCUMCISION TRAY?

The FDA product code for MEDSURG CIRCUMCISION TRAY is HFK.

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Other records listing Medsurg 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.

K920780MEDSURG INSERTION TRAYK940175MEDSURG STERILE O.R. TOWELSK934731MEDSURG STERILE IMAGING PRODUCTSK925558INFILTUBEK934971STERILE LAPAROTOMY SPONGESK920421MEDSURG MARSHMALLOW TRAY

View all 41 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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