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FDA 510(k)

DRG REACTION CHAMBER/SAFETY TIP

K-Number: K012003 · 2002-02-12

Decision Date2002-02-12
Product CodeHEI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DRG REACTION CHAMBER/SAFETY TIP is the device name listed in this FDA 510(k) record. The listed applicant is Doctor'S Research Group, Inc.. It received FDA 510(k) clearance on 2002-02-12 under 510(k) number K012003. The device is classified under product code HEI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRG REACTION CHAMBER/SAFETY TIP?

DRG REACTION CHAMBER/SAFETY TIP is a medical device that received FDA 510(k) clearance on 2002-02-12. The listed applicant is Doctor'S Research Group, Inc.. The 510(k) number is K012003.

When did DRG REACTION CHAMBER/SAFETY TIP receive FDA 510(k) clearance?

DRG REACTION CHAMBER/SAFETY TIP received FDA 510(k) clearance on 2002-02-12, under 510(k) number K012003.

Who is the listed applicant for DRG REACTION CHAMBER/SAFETY TIP?

The FDA 510(k) record lists Doctor'S Research Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRG REACTION CHAMBER/SAFETY TIP?

The FDA product code for DRG REACTION CHAMBER/SAFETY TIP is HEI.

Related Clinical Trials

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.

Other records listing Doctor'S Research Group, 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.

View all 13 devices →

Related Devices (Code: HEI)

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.

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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