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FDA 510(k)

MONOJECT SAMPLETTE CAPILLARY SERUM SEP

K-Number: K823176 · 1982-11-22

ApplicantSherwood Medical Co.
Decision Date1982-11-22
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MONOJECT SAMPLETTE CAPILLARY SERUM SEP is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1982-11-22 under 510(k) number K823176. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOJECT SAMPLETTE CAPILLARY SERUM SEP?

MONOJECT SAMPLETTE CAPILLARY SERUM SEP is a medical device that received FDA 510(k) clearance on 1982-11-22. The listed applicant is Sherwood Medical Co.. The 510(k) number is K823176.

When did MONOJECT SAMPLETTE CAPILLARY SERUM SEP receive FDA 510(k) clearance?

MONOJECT SAMPLETTE CAPILLARY SERUM SEP received FDA 510(k) clearance on 1982-11-22, under 510(k) number K823176.

Who is the listed applicant for MONOJECT SAMPLETTE CAPILLARY SERUM SEP?

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

What is the FDA product code for MONOJECT SAMPLETTE CAPILLARY SERUM SEP?

The FDA product code for MONOJECT SAMPLETTE CAPILLARY SERUM SEP is JKA.

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Other records listing Sherwood Medical Co. as applicant

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Related Devices (Code: JKA)

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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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