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FDA 510(k)

SMART KLAMP VARIOUS BY SIZE

K-Number: K032091 · 2004-03-08

ApplicantEmergogroup, Inc.
Decision Date2004-03-08
Product CodeHFX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SMART KLAMP VARIOUS BY SIZE is the device name listed in this FDA 510(k) record. The listed applicant is Emergogroup, Inc.. It received FDA 510(k) clearance on 2004-03-08 under 510(k) number K032091. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMART KLAMP VARIOUS BY SIZE?

SMART KLAMP VARIOUS BY SIZE is a medical device that received FDA 510(k) clearance on 2004-03-08. The listed applicant is Emergogroup, Inc.. The 510(k) number is K032091.

When did SMART KLAMP VARIOUS BY SIZE receive FDA 510(k) clearance?

SMART KLAMP VARIOUS BY SIZE received FDA 510(k) clearance on 2004-03-08, under 510(k) number K032091.

Who is the listed applicant for SMART KLAMP VARIOUS BY SIZE?

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

What is the FDA product code for SMART KLAMP VARIOUS BY SIZE?

The FDA product code for SMART KLAMP VARIOUS BY SIZE is HFX.

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Other records listing Emergogroup, 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.

K042917STAT MEDICAL PEN NEEDLE

Related Devices (Code: HFX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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