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FDA 510(k)

NEEDLE & BLADE COUNTER & DISPOSAL UNIT

K-Number: K872313 · 1987-07-02

Decision Date1987-07-02
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLE & BLADE COUNTER & DISPOSAL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Gary Plastic Packaging Corp.. It received FDA 510(k) clearance on 1987-07-02 under 510(k) number K872313. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE & BLADE COUNTER & DISPOSAL UNIT?

NEEDLE & BLADE COUNTER & DISPOSAL UNIT is a medical device that received FDA 510(k) clearance on 1987-07-02. The listed applicant is Gary Plastic Packaging Corp.. The 510(k) number is K872313.

When did NEEDLE & BLADE COUNTER & DISPOSAL UNIT receive FDA 510(k) clearance?

NEEDLE & BLADE COUNTER & DISPOSAL UNIT received FDA 510(k) clearance on 1987-07-02, under 510(k) number K872313.

Who is the listed applicant for NEEDLE & BLADE COUNTER & DISPOSAL UNIT?

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

What is the FDA product code for NEEDLE & BLADE COUNTER & DISPOSAL UNIT?

The FDA product code for NEEDLE & BLADE COUNTER & DISPOSAL UNIT is MMK.

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.

Related Devices (Code: MMK)

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

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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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