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FDA 510(k)

ACTION PAC

K-Number: K851276 · 1985-05-15

ApplicantSouth Mountain Medical
Decision Date1985-05-15
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACTION PAC is the device name listed in this FDA 510(k) record. The listed applicant is South Mountain Medical. It received FDA 510(k) clearance on 1985-05-15 under 510(k) number K851276. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTION PAC?

ACTION PAC is a medical device that received FDA 510(k) clearance on 1985-05-15. The listed applicant is South Mountain Medical. The 510(k) number is K851276.

When did ACTION PAC receive FDA 510(k) clearance?

ACTION PAC received FDA 510(k) clearance on 1985-05-15, under 510(k) number K851276.

Who is the listed applicant for ACTION PAC?

The FDA 510(k) record lists South Mountain Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTION PAC?

The FDA product code for ACTION PAC is LDQ.

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.

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Other records listing South Mountain Medical 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.

K853742GAUZE SPONGEK852945HUCK TOWELK831806SUTURE KITS STERILIZED W/GAMA RADIATIONK823485SURE SNIPK812992SURGICAL MASKK811769LAPAROTOMY PADS

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Related Devices (Code: LDQ)

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.

K993797EC-7701 FLUID WARMING CABINETEnthermics Medical Systems, Inc.K992258HOT SHOT FLUID WARMER IV FLUIDSInfra-Med Technologies, Inc.K981032PIV SYSTEMMedical Solutions, Inc.K973747CONTROLLED TEMPERATURE CABINET SYSTEMSmithK955661ACU-HALTGlederer & Co., Inc.K955776ACU-LABGlederer & Co., Inc.

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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