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FDA 510(k)

STERILE BASIN SETS

K-Number: K813012 · 1981-11-06

ApplicantMedspec Corp.
Decision Date1981-11-06
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE BASIN SETS is the device name listed in this FDA 510(k) record. The listed applicant is Medspec Corp.. It received FDA 510(k) clearance on 1981-11-06 under 510(k) number K813012. 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 STERILE BASIN SETS?

STERILE BASIN SETS is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is Medspec Corp.. The 510(k) number is K813012.

When did STERILE BASIN SETS receive FDA 510(k) clearance?

STERILE BASIN SETS received FDA 510(k) clearance on 1981-11-06, under 510(k) number K813012.

Who is the listed applicant for STERILE BASIN SETS?

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

What is the FDA product code for STERILE BASIN SETS?

The FDA product code for STERILE BASIN SETS is LDQ.

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Other records listing Medspec Corp. 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.

K812707STERILE DISSECTOR SPONGES-X-RAY DETECTK812711STERILE GAUZE PADS 12PLYK812710STERILE LAPAROTOMY SPONGES-X-RAY DETECTK812709STERILE DENTAL ROLLK810071STERILE SILICONE TUBINGK810069STERILE AIRWAY

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Related Devices (Code: LDQ)

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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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