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FDA 510(k)

HEMOPHILUS ID QUAD PLATE

K-Number: K870636 · 1987-04-14

ApplicantHardy Media
Decision Date1987-04-14
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HEMOPHILUS ID QUAD PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Media. It received FDA 510(k) clearance on 1987-04-14 under 510(k) number K870636. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOPHILUS ID QUAD PLATE?

HEMOPHILUS ID QUAD PLATE is a medical device that received FDA 510(k) clearance on 1987-04-14. The listed applicant is Hardy Media. The 510(k) number is K870636.

When did HEMOPHILUS ID QUAD PLATE receive FDA 510(k) clearance?

HEMOPHILUS ID QUAD PLATE received FDA 510(k) clearance on 1987-04-14, under 510(k) number K870636.

Who is the listed applicant for HEMOPHILUS ID QUAD PLATE?

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

What is the FDA product code for HEMOPHILUS ID QUAD PLATE?

The FDA product code for HEMOPHILUS ID QUAD PLATE is JSH.

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Other records listing Hardy Media 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.

K880134MIDDLEBROOK 7H11 AGARK880122MIDDLEBROOK 7H9 BROTHK880131LOWENSTEIN-JENSEN, GRUFTK880133MIL MEDIUMK880126LAURYL TRYPTOSE BROTHK880116MRVP BROTH

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Related Devices (Code: JSH)

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.

K881551PHENOL RED BROTH BASEAcumedia Manufacturers, Inc.K881553RUSSELL DOUBLE SUGAR AGARAcumedia Manufacturers, Inc.K881486DNASE TEST AGARAcumedia Manufacturers, Inc.K881540FLO AGARAcumedia Manufacturers, Inc.K881559UREA AGAR BASEAcumedia Manufacturers, Inc.K881560UREA BROTHAcumedia Manufacturers, 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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