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FDA 510(k)

PROCEDURE PACKS SOLUTION ADMINISTRATION SETS

K-Number: K882716 · 1988-09-16

ApplicantProcedure Packs, Inc.
Decision Date1988-09-16
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PROCEDURE PACKS SOLUTION ADMINISTRATION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Procedure Packs, Inc.. It received FDA 510(k) clearance on 1988-09-16 under 510(k) number K882716. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCEDURE PACKS SOLUTION ADMINISTRATION SETS?

PROCEDURE PACKS SOLUTION ADMINISTRATION SETS is a medical device that received FDA 510(k) clearance on 1988-09-16. The listed applicant is Procedure Packs, Inc.. The 510(k) number is K882716.

When did PROCEDURE PACKS SOLUTION ADMINISTRATION SETS receive FDA 510(k) clearance?

PROCEDURE PACKS SOLUTION ADMINISTRATION SETS received FDA 510(k) clearance on 1988-09-16, under 510(k) number K882716.

Who is the listed applicant for PROCEDURE PACKS SOLUTION ADMINISTRATION SETS?

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

What is the FDA product code for PROCEDURE PACKS SOLUTION ADMINISTRATION SETS?

The FDA product code for PROCEDURE PACKS SOLUTION ADMINISTRATION SETS is DQD.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Procedure Packs, 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.

K891572ANGIOGRAPHY CUSTOM PACKSK882717PROCEDURE PACKS CONTRAST MEDIA SETSK882655PROCEDURE PACKS PRESS. MONITOR/ADMINISTRATION LINE

Related Devices (Code: DQD)

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.

K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730)Shanghai Hulu Devices Co., Ltd.K261694CORE 300 Digital StethoscopeEko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089Tyto Stethoscope (G3)Tyto Care , Ltd.K252076Kneevoice Cartilage Evaluation System (750-3600-001)Kneevoice, Inc.K252284eMurmur Heart AICsd Labs

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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